Identity
- Trade Name
- VERTEBRIS FDA UDI
- Generic Name
- Spinal rongeur FDA UDI
- Device Name
- RONGEUR Ø 2.6MM WL 360MM color code orange, TL 457 mm, with irrigation connection, reusable FDA UDI
- Model / Reference
- 892401125 FDA UDI
- Description
- RONGEUR Ø 2.6MM WL 360MM color code orange, TL 457 mm, with irrigation connection, reusable FDA UDI
Identifiers
- Catalog Number
- 89240.1125 FDA UDI
- Primary DI / UDI-DI
- 04055207035481 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Spinal rongeur FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 2.6 Millimeter FDA UDILength — 360 Millimeter FDA UDI
Vertebris by Richard Wolf GmbH — 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 |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI e476f0eb-fcc0-4b9b-941a-e0b156140401 37 fields · synced May 31, 2026