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Disposable Backflush instrument, with blunt needle and passive aspiration.(20 ga
FDA UDIClass I (US FDA UDI)
by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
Identity
- Trade Name
- Disposable Backflush instrument, with blunt needle and passive aspiration.(20 ga FDA UDI
- Generic Name
- Vitrectomy fluid/gas handling handpiece/cannula FDA UDI
- Device Name
- Disposable Backflush instrument, with blunt needle and passive aspiration.(20 gauge / 0.9 mm) FDA UDI
- Model / Reference
- 1281.AD FDA UDI
- Description
- Disposable Backflush instrument, with blunt needle and passive aspiration.(20 gauge / 0.9 mm) FDA UDI
Identifiers
- Catalog Number
- 1281.AD FDA UDI
- Primary DI / UDI-DI
- 08717872003603 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
Disposable Backflush instrument, with blunt needle and passive aspiration.(20 ga by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I…
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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
Sources (1)
- FDA UDI 3f4ca3fb-600b-4c29-b51e-14cefb2145b8 34 fields · synced May 31, 2026