Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Manual surgical saw blade, flexible, reusable FDA UDI
- Device Name
- DAVIS CONDUCTOR FOR GIGLI SAW OVERALL LENGTH 8-1/4 inches21CM FDA UDI
- Model / Reference
- NL750 FDA UDI
- Description
- DAVIS CONDUCTOR FOR GIGLI SAW OVERALL LENGTH 8-1/4 inches21CM FDA UDI
Identifiers
- Catalog Number
- NL750 FDA UDI
- Primary DI / UDI-DI
- 10885403070440 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
Similar devices
Also classified as Manual surgical saw blade, flexible, reusable.
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Integra® Ruggles®-Redmond™ — Integra LifeSciences Production Corporation · Class I
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- Symmetry Surgical — SYMMETRY SURGICAL INC. · Class I
- Symmetry Strully Gigli — SYMMETRY SURGICAL INC. · Class I
- 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI b12393c1-126c-46c4-b7d6-b1bd4ffa8f4f 35 fields · synced Jun 6, 2026