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ProSilver

FDA UDI

Class II (US FDA UDI)

by Silmet Ltd

Identity

Trade Name
ProSilver FDA UDI
Generic Name
Dental amalgam FDA UDI
Device Name
Dental Amalgam Alloy FDA UDI
Model / Reference
P-110471 FDA UDI
Description
Dental Amalgam Alloy FDA UDI

Identifiers

Catalog Number
P-110471 FDA UDI
Primary DI / UDI-DI
07290012207693 FDA UDI
FDA Product Code
EJJ FDA UDI
GMDN Term
Dental amalgam FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3070 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 amalgam

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

Similar devices

Also classified as Dental amalgam.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Silmet Ltd

Sources (1)

  • FDA UDI 56a7785c-5251-4268-993a-f5e0dc60c991 34 fields · synced Jun 8, 2026