← Back to catalogue

Stoma®

FDA UDI

Class I (US FDA UDI)

by Storz am Mark GmbH

Identity

Trade Name
STOMA® FDA UDI
Generic Name
General-purpose bowl, reusable FDA UDI
Device Name
Metal Dish, 140ccm, 80mmx40mm FDA UDI
Model / Reference
6939.08 FDA UDI
Description
Metal Dish, 140ccm, 80mmx40mm FDA UDI

Identifiers

Catalog Number
6939.08 FDA UDI
Primary DI / UDI-DI
ESAM6939081 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
General-purpose bowl, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: General-purpose bowl, reusable

Stoma® by Storz am Mark GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose bowl, 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
Storz am Mark GmbH

Sources (1)

  • FDA UDI 717028a4-2e2d-4936-98b8-946a39b1d956 35 fields · synced May 30, 2026