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Surgical Direct

FDA UDI

Class I (US FDA UDI)

by Surgical Direct, Inc.

Identity

Trade Name
Surgical Direct FDA UDI
Generic Name
Lacrimal procedural cannula FDA UDI
Device Name
1 3/4" Osher "J" Cannula, 27 Gauge With 2.25mm Wide and 2.25mm Long "J" Tip FDA UDI
Model / Reference
S34713.100 FDA UDI
Description
1 3/4" Osher "J" Cannula, 27 Gauge With 2.25mm Wide and 2.25mm Long "J" Tip FDA UDI

Identifiers

Catalog Number
S34713.100 FDA UDI
Primary DI / UDI-DI
B382S347131000 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Lacrimal procedural cannula 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

No

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: Lacrimal procedural cannula

Surgical Direct by Surgical Direct, Inc. — Class I — 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
Surgical Direct, Inc.

Sources (1)

  • FDA UDI 20b15094-32f8-42e9-a2b2-8a5bbd1c9a8e 35 fields · synced May 30, 2026