Identity
- Trade Name
- IH-Papain FDA UDI
- Generic Name
- Papain immunohaematology reagent IVD FDA UDI
- Device Name
- IH-Papain; 1 x 5mL vial lyophilized FDA UDI
- Model / Reference
- 813540100 FDA UDI
- Description
- IH-Papain; 1 x 5mL vial lyophilized FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07611969952199 FDA UDI
- FDA Product Code
- KSK FDA UDI
- GMDN Term
- Papain immunohaematology reagent IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
Yes
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
Category: Papain immunohaematology reagent IVD
IH-Papain by Bio-Rad Medical Diagnostics GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Papain immunohaematology reagent IVD.
- Papain — DIAGAST · Class II
- ALBAzyme™ Papain Solution Kit — ALBA BIOSCIENCE LIMITED · Class II
- ORTHOTM Sera Papain — ALBA BIOSCIENCE LIMITED · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bio-Rad Medical Diagnostics GmbH
Sources (1)
- FDA UDI 8b2c528c-5219-4274-bf99-fa7c7c2d51a6 34 fields · synced May 31, 2026