← Back to catalogue
Backflush Needle with tapered tip from 23 gauge/0.6 mm to 27 gauge/0.4 mm
FDA UDIClass I (US FDA UDI)
by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Identity
- Trade Name
- Backflush Needle with tapered tip from 23 gauge/0.6 mm to 27 gauge/0.4 mm FDA UDI
- Generic Name
- Vitrectomy fluid/gas handling handpiece/cannula FDA UDI
- Device Name
- Backflush Needle with tapered tip from 23 gauge/0.6 mm to 27 gauge/0.4 mm and luer lock connector for use with 1281.C handpiece. FDA UDI
- Model / Reference
- 1281.CD27 FDA UDI
- Description
- Backflush Needle with tapered tip from 23 gauge/0.6 mm to 27 gauge/0.4 mm and luer lock connector for use with 1281.C handpiece. FDA UDI
Identifiers
- Catalog Number
- 1281.CD27 FDA UDI
- Primary DI / UDI-DI
- 08717872016092 FDA UDI
- FDA Product Code
- HMX FDA UDI
- GMDN Term
- Vitrectomy fluid/gas handling handpiece/cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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
No
FDA UDI
Category: Vitrectomy fluid/gas handling handpiece/cannula
Backflush Needle with tapered tip from 23 gauge/0.6 mm to 27 gauge/0.4 mm by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I — FDA…
Similar devices
Also classified as Vitrectomy fluid/gas handling handpiece/cannula.
- Bausch + Lomb — Bausch & Lomb Incorporated · Class II
- VitreQ — Vitreq B.V. · Class I
- Vortex Surgical Inc — Vortex Surgical, Inc. · Class I
- VitreQ — Vitreq B.V. · Class I
- Vortex Surgical Inc — Vortex Surgical, Inc. · Class I
- Bausch + Lomb — Bausch & Lomb Incorporated · Class II
- Bausch + Lomb — Bausch & Lomb Incorporated · Class II
- Vortex Surgical Inc — Vortex 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
Sources (1)
- FDA UDI 19738bbe-4d47-4047-8be9-40c9c9b95c05 34 fields · synced Jun 6, 2026