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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 working-channel cannula, single-use FDA UDI
Device Name
Hovis Hydrodissection Cannula, 27g x 7/8” (0.4 x 22mm), 4mm Bend FDA UDI
Model / Reference
B-4036D-NSC FDA UDI
Description
Hovis Hydrodissection Cannula, 27g x 7/8” (0.4 x 22mm), 4mm Bend FDA UDI

Identifiers

Primary DI / UDI-DI
10845819006365 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic working-channel cannula, 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 working-channel cannula, single-use

A reusable cannula for creating channels in the sclera for internal ocular access during posterior segment ophthalmic surgery. It is designed to be used once and is typically made of plastic materials or high-grade stainless steel.

Similar devices

Also classified as Ophthalmic working-channel cannula, 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 9934ec2a-2d54-4380-8a1c-670a53b449d1 34 fields · synced Aug 4, 2026