flow.sil Assortment

FDA UDI

Class I (US FDA UDI)

by bredent GmbH & Co. KG

Identity

Trade Name: flow.sil Assortment FDA UDI
Generic Name: Denture reliner, soft, professional FDA UDI
Device Name: flow.sil Assortment 10 parts 1 Assortment FDA UDI
Model / Reference: 54001270 FDA UDI
Description: flow.sil Assortment 10 parts 1 Assortment FDA UDI

Identifiers

Catalog Number: 54001270 FDA UDI
Primary DI / UDI-DI: EBRE540012700 FDA UDI
FDA Product Code: EFX FDA UDI
GMDN Term: Denture reliner, soft, professional FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6670 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Denture reliner, soft, professional

flow.sil Assortment by bredent GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: bredent GmbH & Co. KG

Sources (1)

FDA UDI 0c2f5069-c7e4-428c-a7eb-596df55ad54b 35 fields · synced May 31, 2026