← Back to catalogue

Stoma®

FDA UDI

Class I (US FDA UDI)

by Storz am Mark GmbH

Identity

Trade Name
STOMA® FDA UDI
Generic Name
Dental suction system cannula, reusable FDA UDI
Device Name
Suction pipe, Ø 4mm, 14cm FDA UDI
Model / Reference
3334.15 FDA UDI
Description
Suction pipe, Ø 4mm, 14cm FDA UDI

Identifiers

Catalog Number
3334.15 FDA UDI
Primary DI / UDI-DI
ESAM3334151 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Dental suction system cannula, 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: Dental suction system cannula, reusable

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

Similar devices

Also classified as Dental suction system 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
Storz am Mark GmbH

Sources (1)

  • FDA UDI cb84d852-7ee3-4afa-8243-51ce6065f130 35 fields · synced Jun 1, 2026