← Back to catalogue

Hydrodissection Cannulae

FDA UDI

Class II (US FDA UDI)

by Sterimedix Limited

Identity

Trade Name
Hydrodissection Cannulae FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
27g TW x 22mm Akahoshi FDA UDI
Model / Reference
M3919-02/10 FDA UDI
Description
27g TW x 22mm Akahoshi FDA UDI

Identifiers

Catalog Number
M3919 FDA UDI
Primary DI / UDI-DI
15056030400909 FDA UDI
FDA Product Code
MED FDA UDI
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6885 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
Sterilization Method
Ethylene Oxide FDA UDI

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

Hydrodissection Cannulae by Sterimedix Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
Sterimedix Limited

Sources (1)

  • FDA UDI 575905c8-791d-4878-b946-c610851f162a 34 fields · synced Jun 8, 2026