Identity
- Trade Name
- VERTEBRIS FDA UDI
- Generic Name
- Endoscope sheath, reusable FDA UDI
- Device Name
- WORKING SLEEVE ID 6MM OD 7MM TL 186MM TL 186 mm, distal end with 45° fenestration, graduated, reusable FDA UDI
- Model / Reference
- 892201037 FDA UDI
- Description
- WORKING SLEEVE ID 6MM OD 7MM TL 186MM TL 186 mm, distal end with 45° fenestration, graduated, reusable FDA UDI
Identifiers
- Catalog Number
- 89220.1037 FDA UDI
- Primary DI / UDI-DI
- 04055207046692 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Endoscope sheath, reusable 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 — 7 Millimeter FDA UDILength — 186 Millimeter FDA UDILumen/Inner Diameter — 6 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 c858e1c9-dff8-4852-8b31-5397fd7fe9c9 37 fields · synced May 31, 2026