← Back to catalogue
Keratin 14 Polyclonal Antibody, Purified
EUDAMEDFDA UDIClass IVD General (EU MDR)
Ref 905301
Identity
- Trade Name
- Keratin 14 Polyclonal Antibody, Purified. FDA UDI
- Generic Name
- Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry FDA UDI
- Device Name
- Keratin 14 Polyclonal Antibody, Purified EUDAMEDURL: https://www.biolegend.com/en-us/products/keratin-14-polyclonal-antibody-purified-10953 FDA UDI
- Model / Reference
- 905301 EUDAMEDFDA UDI
- Description
- URL: https://www.biolegend.com/en-us/products/keratin-14-polyclonal-antibody-purified-10953 FDA UDI
Identifiers
- Catalog Number
- 905301 FDA UDI
- Primary DI / UDI-DI
- 00810034700049 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00810034700049 EUDAMED
- FDA Product Code
- NJT FDA UDI
- EMDN Code
- W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
- GMDN Term
- Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass I FDA UDI
- Regulation Number
- 864.1860 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 100 Microliter FDA UDI
Keratin 14 Polyclonal Antibody, Purified by Biolegend, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-00810034700049 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BioLegend Inc
- EUDAMED SRN
- US-MF-000013824
- Authorised Representative
- MedEnvoy Global BV NL-AR-000024028
Sources (2)
- EUDAMED d9385586-9921-49de-9f12-d912d50887a0 61 fields · synced Jul 21, 2026
- FDA UDI f72e14ed-60e9-4963-beb9-dcc25fe72e10 37 fields · synced May 30, 2026