Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Manual surgical saw blade, flexible, reusable FDA UDI
- Device Name
- BAILEY CONDUCTOR FOR GIGLI SAW OVERALL LENGTH 13 inches33CM FDA UDI
- Model / Reference
- NL760 FDA UDI
- Description
- BAILEY CONDUCTOR FOR GIGLI SAW OVERALL LENGTH 13 inches33CM FDA UDI
Identifiers
- Catalog Number
- NL760 FDA UDI
- Primary DI / UDI-DI
- 10885403070457 FDA UDI
- FDA Product Code
- HBG FDA UDI
- GMDN Term
- Manual surgical saw blade, flexible, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4300 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: Manual surgical saw blade, flexible, reusable
V. Mueller by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Manual surgical saw blade, flexible, reusable.
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- Symmetry GIGLI — SYMMETRY SURGICAL INC. · Class I
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
- Steris Corporation
Sources (1)
- FDA UDI 558e5cc1-ab9a-4f42-87ab-5e7af6dc0d30 35 fields · synced Jun 8, 2026