Identity
- Trade Name
- Endocuff Vision FDA UDI
- Generic Name
- Colonoscope distal anchoring cuff FDA UDI
- Device Name
- ARV120 Size 2 (L) Endocuff Vision Green Sterilised - 1 pot - single unit FDA UDI
- Model / Reference
- ARV120 FDA UDI
- Description
- ARV120 Size 2 (L) Endocuff Vision Green Sterilised - 1 pot - single unit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060423410171 FDA UDI
- FDA Product Code
- FED FDA UDI
- GMDN Term
- Colonoscope distal anchoring cuff FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 11.2 Millimeter FDA UDI
Category: Colonoscope distal anchoring cuff
Endocuff Vision by Boddingtons Plastics, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Endocuff — Boddingtons Plastics, Ltd. · Class II
- Endocuff Vision — Boddingtons Plastics, Ltd. · Class II
- Endocuff Vision — Boddingtons Plastics, Ltd. · Class II
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
- Boddingtons Plastics, Ltd.
Sources (1)
- FDA UDI fd748143-4ae5-4b3e-8fcb-738307a7ecf2 34 fields · synced Jun 8, 2026