← Back to catalogue

Osher “J” Cannula, 27ga

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Osher “J” Cannula, 27ga FDA UDI
Generic Name
Ophthalmic working-channel cannula, reusable FDA UDI
Device Name
Osher “J” Cannula, 27ga FDA UDI
Model / Reference
1245-27 FDA UDI
Description
Osher “J” Cannula, 27ga FDA UDI

Identifiers

Primary DI / UDI-DI
00840096205732 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic working-channel cannula, reusable 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic working-channel cannula, reusable

Osher “J” Cannula, 27ga by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic working-channel cannula, reusable.

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
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI 8f0bc3c1-24f7-4f72-8ed4-e60204a0d2cd 33 fields · synced May 30, 2026