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ProFil Flow

FDA UDI

Class II (US FDA UDI)

by Silmet Ltd

Identity

Trade Name
ProFil Flow FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Dental Composite Restorative FDA UDI
Model / Reference
SM-163A03 FDA UDI
Description
Dental Composite Restorative FDA UDI

Identifiers

Catalog Number
SM-163A03 FDA UDI
Primary DI / UDI-DI
07290016787511 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

ProFil Flow by Silmet Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Silmet Ltd

Sources (1)

  • FDA UDI c8dfcc28-7c61-4482-960f-312c011b9a26 34 fields · synced Jun 1, 2026