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Backflush instrument with active aspiration 20G / 0.9 mm.

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 active aspiration 20G / 0.9 mm. FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI
Model / Reference
1281.T FDA UDI

Identifiers

Catalog Number
1281.T FDA UDI
Primary DI / UDI-DI
08717872003979 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Backflush instrument with active aspiration 20G / 0.9 mm. by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I — FDA UDI — listed in…

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df216c3d-c769-409b-8c68-91878913712e 33 fields · synced May 30, 2026