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Lachrymal Cannulae

FDA UDI

Class II (US FDA UDI)

by Sterimedix Limited

Identity

Trade Name
Lachrymal Cannulae FDA UDI
Generic Name
Lacrimal procedural cannula FDA UDI
Device Name
26g x 1 1/4" Lachrymal FDA UDI
Model / Reference
M9276-02/10 FDA UDI
Description
26g x 1 1/4" Lachrymal FDA UDI

Identifiers

Catalog Number
M9276 FDA UDI
Primary DI / UDI-DI
35056030402389 FDA UDI
FDA Product Code
MED FDA UDI
GMDN Term
Lacrimal procedural cannula 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: Lacrimal procedural cannula

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

Similar devices

Also classified as Lacrimal procedural cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sterimedix Limited

Sources (1)

  • FDA UDI c5229098-5acd-4f4b-8f0b-2016eeeb510f 34 fields · synced May 30, 2026