Identity
- Trade Name
- BOSS Instruments FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- Pulmonary Artery Clamp, spring shaft, 20mm, 9" FDA UDI
- Model / Reference
- 65-8050 FDA UDI
- Description
- Pulmonary Artery Clamp, spring shaft, 20mm, 9" FDA UDI
Identifiers
- Catalog Number
- 65-8050 FDA UDI
- Primary DI / UDI-DI
- 00888515115637 FDA UDI
- FDA Product Code
- DXC FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4450 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
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
No
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
BOSS Instruments by Boss Instruments, Ltd. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Boss Instruments, Ltd.
Sources (1)
- FDA UDI 2e7079d6-5779-4265-92f7-a442f280f9af 36 fields · synced Jun 9, 2026