Identity
- Trade Name
- BOSS Instruments FDA UDI
- Generic Name
- Neurosurgical curette, reusable FDA UDI
- Device Name
- B-K Micro Lumbar Curette, Backward Down, 1 FDA UDI
- Model / Reference
- 70-7658 FDA UDI
- Description
- B-K Micro Lumbar Curette, Backward Down, 1 FDA UDI
Identifiers
- Catalog Number
- 70-7658 FDA UDI
- Primary DI / UDI-DI
- 00888515163690 FDA UDI
- FDA Product Code
- GZX FDA UDI
- GMDN Term
- Neurosurgical curette, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Neurosurgical curette, reusable
BOSS Instruments by Boss Instruments, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Boss Instruments, Ltd.
Sources (1)
- FDA UDI 1214ec50-ecb9-4d4a-a742-16ca3b7650b7 35 fields · synced Jun 9, 2026