Identity
- Trade Name
- Genemed® FDA UDI
- Generic Name
- Progesterone receptor IVD, antibody FDA UDI
- Device Name
- anti-Progesterone Receptor Rabbit Monoclonal Antibody [Y85], Ready-To-Use, 15 mL FDA UDI
- Model / Reference
- 60-0219-15 FDA UDI
- Description
- anti-Progesterone Receptor Rabbit Monoclonal Antibody [Y85], Ready-To-Use, 15 mL FDA UDI
Identifiers
- Catalog Number
- 60-0219-15 FDA UDI
- Primary DI / UDI-DI
- 00615233008169 FDA UDI
- FDA Product Code
- MVU FDA UDI
- GMDN Term
- Progesterone receptor IVD, antibody FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.4020 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Category: Progesterone receptor IVD, antibody
Genemed® by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Progesterone receptor IVD, antibody.
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- QSX-Enh-P PR (ASR) — NOVODIAX, INC. · Class I
- Anti-PR (Insite) — Biogenex Laboratories, Inc. · Class II
- Anti-PR (Insite) — Biogenex Laboratories, Inc. · Class II
- CONFIRM antiProgesterone Receptor PR 1E2 Rabbit Monoclonal Primary Antibody — Ventana Medical Systems · Class II
- Anti-PR (Insite) — Biogenex Laboratories, Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Sakura Finetek USA, Inc
Sources (1)
- FDA UDI ae1f1d12-d014-459a-bd5c-1955cf3f4d9f 35 fields · synced May 30, 2026