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OstomyGel

FDA UDI

Class I (US FDA UDI)

by Dmc Importacao E Exportacao De Equipamentos Ltda

Identity

Trade Name
OstomyGel FDA UDI
Generic Name
Ostomy odour-absorbent/deodorizer FDA UDI
Device Name
Ostomy accessory FDA UDI
Model / Reference
290010003 FDA UDI
Description
Ostomy accessory FDA UDI

Identifiers

Catalog Number
290010003 FDA UDI
Primary DI / UDI-DI
07898616351431 FDA UDI
FDA Product Code
GDS FDA UDI
GMDN Term
Ostomy odour-absorbent/deodorizer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ostomy odour-absorbent/deodorizer

OstomyGel by Dmc Importacao E Exportacao De Equipamentos Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ostomy odour-absorbent/deodorizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dmc Importacao E Exportacao De Equipamentos Ltda

Sources (1)

  • FDA UDI d61d517c-a448-4c78-a133-8b38918a23ad 34 fields · synced May 30, 2026