Identity
- Trade Name
- BI-OK Steam Vials (20/pack) FDA UDI
- Generic Name
- Biological sterilization indicator FDA UDI
- Device Name
- BI-OK Steam Vials (20/pack) FDA UDI
- Model / Reference
- 26920000 FDA UDI
- Description
- BI-OK Steam Vials (20/pack) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30818087012332 FDA UDI
- 510(k) Number
- K891784 FDA UDI
- FDA Product Code
- FRC FDA UDI
- GMDN Term
- Biological sterilization indicator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2800 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Biological sterilization indicator
BI-OK Steam Vials (20/pack) by Propper Manufacturing Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K891784 also covers:
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 |
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Manufacturer
- Manufacturer
- Propper Manufacturing Co., Inc.
Sources (1)
- FDA UDI c60a8d84-ad6c-47b1-b690-e7947b3e6f3f 34 fields · synced Jun 6, 2026