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Anaesthetic Needles

FDA UDI

Class II (US FDA UDI)

by Sterimedix Limited

Identity

Trade Name
Anaesthetic Needles FDA UDI
Generic Name
Ophthalmic needle, single-use FDA UDI
Device Name
25g x 1 1/4" Peribulbar FDA UDI
Model / Reference
0642-03/Y FDA UDI
Description
25g x 1 1/4" Peribulbar FDA UDI

Identifiers

Catalog Number
M0642 FDA UDI
Primary DI / UDI-DI
05056030400162 FDA UDI
FDA Product Code
MED FDA UDI
GMDN Term
Ophthalmic needle, 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 needle, single-use

Anaesthetic Needles by Sterimedix Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sterimedix Limited

Sources (1)

  • FDA UDI 72d2d6f0-f6ec-4177-b3e4-d44aabecab38 34 fields · synced Jun 8, 2026