Identity
- Trade Name
- Biotrol FDA UDI
- Generic Name
- Medical device disinfection agent FDA UDI
- Device Name
- BIOZYME-LT 32 OZ BOTTLE FDA UDI
- Model / Reference
- BLT900 FDA UDI
- Description
- BIOZYME-LT 32 OZ BOTTLE FDA UDI
Identifiers
- Catalog Number
- BLT900 FDA UDI
- Primary DI / UDI-DI
- 00302730000368 FDA UDI
- FDA Product Code
- LRJ FDA UDI
- GMDN Term
- Medical device disinfection agent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6890 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Biotrol by Young Dental Manufacturing I, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Young Dental Manufacturing I, Llc
Sources (1)
- FDA UDI 69ebd112-d5af-4505-a8a3-dc7810d09942 36 fields · synced Jun 6, 2026