URL for Loctite material approvals

somashekar

Staff member
Admin
#1
THIS is the URL where you can check the availability of approvals for any of Loctite materials.
I am sure this will be handy to many design engineers as well as purchase engineers. Came across this today when searching for medical grade RTV's...
Use the designated 4 digit product code for the Product name (Ex. 5240)
:agree:
 
Last edited:
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
somashekar GMP (Good Manufacturing Practices) essential information URL Manufacturing and Related Processes 1
Marc Google URL Index Hits 1 Trillion World News 6
E Layouts : Can you "verify" things that are not visible (such as loctite present, internal dimensions) in a layout ? APQP and PPAP 2
P Loctite as Manufacturing Material use in Medical Device Assemblies 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 12
S QA issues with variations in the viscosity of Henkel's Loctite 480 "rubberized" C.A. Manufacturing and Related Processes 2
T Shrinkage Testing for EPDM Material Various Other Specifications, Standards, and related Requirements 5
M Preparing a document for Raw Material of Medical Device EU Medical Device Regulations 1
J ISO 13485- 8.3.1 Non-conforming material high volume ISO 13485:2016 - Medical Device Quality Management Systems 4
Awais Taking Pictures of Outbound Material - In the Manufacturing Shop floor Manufacturing and Related Processes 5
Q G11 material Manufacturing and Related Processes 7
M Medical Device Marketing Material - Control of Social Media 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
M Origin of Material Review Board AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
D Raw Material Expirations Manufacturing and Related Processes 2
W What is okay to use as a reference material for ISO 17025? ISO 17025 related Discussions 4
J Scrap Material Scale Calibration Required? IATF 16949 - Automotive Quality Systems Standard 21
R Revalidation under VDmax25 following material change ISO 13485:2016 - Medical Device Quality Management Systems 2
J Example of a defined procedure for carrying out Material Review Board (MRB) Manufacturing and Related Processes 0
S Advice on how to reduce overhead of handling non-conforming material Nonconformance and Corrective Action 7
R AS9102 FAI Change in Material / Process Supplier AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
S Predicate Material 510(k) US Food and Drug Administration (FDA) 1
S Predicate Material 510(k) Medical Device and FDA Regulations and Standards News 3
lanley liao Who can share these material with me ? Training - Internal, External, Online and Distance Learning 1
E Record Retention - Raw Material (Steel Certs) Records and Data - Quality, Legal and Other Evidence 3
M Documents to be included in 1.3 Material check in PPA report APQP and PPAP 4
rerusk1 MRB (Material Review Board) Process using MS Sharepoint or MS Teams Manufacturing and Related Processes 2
M Material incoming to the production process reflected in PFMEA FMEA and Control Plans 9
R Do we need issue ECN (Engineering Change Notice) towards updated Material Specification? Design and Development of Products and Processes 2
Q Change the shape of the raw material FAI AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
S Regrind Material in Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 1
Anonymous16-2 Dietary Supplement Raw Material/Component Storage and Production Manufacturing and Related Processes 1
H Expired packaging material - Expired unused Tyvek pouches Other Medical Device and Orthopedic Related Topics 2
A Design History File - Not ready to share the design drawings or Bill of Material US Food and Drug Administration (FDA) 2
D Class 3 Device - Change of supplier of material Canada Medical Device Regulations 6
D List A IVD - Change to material supplier EU Medical Device Regulations 3
Skooma Deburring and Tolerances - Is there a Standard for deburring or removing material? Manufacturing and Related Processes 3
D Can PFMEA be used in disposition of NC material? ISO 14971 - Medical Device Risk Management 4
DuncanGibbons Manufacturing Plan vs Material Specification vs Control Plan Manufacturing and Related Processes 5
Jane's Like-for-like critical raw material change qualification - type of testing/ number of lots required ISO 13485:2016 - Medical Device Quality Management Systems 4
L AS5553 Clause 3.1.7 e "Control packaging material ..................reused" AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
J Raw material certificates - CC - Safety products - Sheet metal stamping IATF 16949 - Automotive Quality Systems Standard 1
C Manufacturing overages & nonconforming material documentation ISO 13485:2016 - Medical Device Quality Management Systems 3
M Changing supplier of critical raw material (III class device) Other Medical Device and Orthopedic Related Topics 1
I Where can I beg, steal (just kidding of course) or borrow good training material on the ISO 9001:2015 standard? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
DMLqms Material for laboratory use or Medical Device? EU Medical Device Regulations 2
C Material from outside CER evaluation period CE Marking (Conformité Européene) / CB Scheme 8
F AS9100D, raw material standards are a requirement for manufacturing? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
6 Management of SDS and Hazardous Material Occupational Health & Safety Management Standards 2
L ASQ CBA biomedical auditor - CBA primer material is enough to study? ISO 13485:2016 - Medical Device Quality Management Systems 6
DuncanGibbons Are there any aerospace specific requirements for material resource planning? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
T Was Just told we could ONLY buy material for AS9100 customers if the DISTRIBUTION house is AS9100 / AS9120 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3

Similar threads

Top Bottom