← Back to catalogue

Backflush Instrument with 20 gauge / 0.9 mm brush needle.

FDA UDI

Class I (US FDA UDI)

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Identity

Trade Name
Backflush Instrument with 20 gauge / 0.9 mm brush needle. FDA UDI
Generic Name
Vitrectomy fluid/gas handling handpiece/cannula FDA UDI
Model / Reference
2281.BD FDA UDI

Identifiers

Catalog Number
2281.BD FDA UDI
Primary DI / UDI-DI
08717872026145 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 Instrument with 20 gauge / 0.9 mm brush needle. by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I — FDA UDI — listed in…

Similar devices

Also classified as Vitrectomy fluid/gas handling handpiece/cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Sources (1)

  • FDA UDI 3105bee7-5f76-462f-a1f8-693834bb6231 33 fields · synced May 30, 2026