Identity
- Trade Name
- BARS Anchor black FDA UDI
- Generic Name
- Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
- Device Name
- The application aid BARS Anchor is an anchor-shaped instrument for the fixation of tissue when using flexible endoscopes in conjunction with the BARS Set. The BARS Anchor is available in two colours for better differentiation when using several instruments: spiral slotted tube in black (BARS Anchor black - 200.13) or in silver (BARS Anchor silver - 200.12). The Anchor needles are made of Nitinol. FDA UDI
- Model / Reference
- 165 cm FDA UDI
- Description
- The application aid BARS Anchor is an anchor-shaped instrument for the fixation of tissue when using flexible endoscopes in conjunction with the BARS Set. The BARS Anchor is available in two colours for better differentiation when using several instruments: spiral slotted tube in black (BARS Anchor black - 200.13) or in silver (BARS Anchor silver - 200.12). The Anchor needles are made of Nitinol. FDA UDI
Identifiers
- Catalog Number
- 200.13 FDA UDI
- Primary DI / UDI-DI
- 04260206311270 FDA UDI
- FDA Product Code
- PTS FDA UDI
- GMDN Term
- Flexible endoscopic tissue manipulation forceps, single-use 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Flexible endoscopic tissue manipulation forceps, single-use
BARS Anchor black by Ovesco Endoscopy AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible endoscopic tissue manipulation forceps, single-use.
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ovesco Endoscopy AG
Sources (1)
- FDA UDI c1e2b0f9-29ba-4fb5-bde3-399a3aa2a352 36 fields · synced Jun 8, 2026