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Disposable Instruments

FDA UDI

Class I (US FDA UDI)

by OASIS Medical, Inc.

Identity

Trade Name
Disposable Instruments FDA UDI
Generic Name
Ophthalmic surgical irrigation/infusion/aspiration handle, single-use FDA UDI
Device Name
Anterior Chamber Cannula, 27g x 7/8” (0.4 x 22mm), 8mm Bend (bulk, non-sterile) FDA UDI
Model / Reference
B-4002B-NSC FDA UDI
Description
Anterior Chamber Cannula, 27g x 7/8” (0.4 x 22mm), 8mm Bend (bulk, non-sterile) FDA UDI

Identifiers

Primary DI / UDI-DI
20845819001442 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic surgical irrigation/infusion/aspiration handle, single-use 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

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: Ophthalmic surgical irrigation/infusion/aspiration handle, single-use

A comprehensive and accurate overview of the Disposable Instruments medical device, including its purpose, features, compliance, and frequently asked questions.

Similar devices

Also classified as Ophthalmic surgical irrigation/infusion/aspiration handle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
OASIS Medical, Inc.

Sources (1)

  • FDA UDI 3ac1c637-0cb7-4820-8fd5-086301df892c 34 fields · synced Jul 9, 2026