← Back to catalogue

No Brand

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
No Brand FDA UDI
Generic Name
Rigid endoscopic cannula, reusable FDA UDI
Device Name
SHORT OBTURATOR FDA UDI
Model / Reference
E0014838-6 FDA UDI
Description
SHORT OBTURATOR FDA UDI

Identifiers

Catalog Number
E0014838-6 FDA UDI
Primary DI / UDI-DI
00885556646892 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Rigid endoscopic cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Rigid endoscopic cannula, reusable

No Brand by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic 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
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI d036358a-c6a2-4d3c-bcb7-482b97f12153 35 fields · synced Jun 8, 2026