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Reprosil® Hydrophilic Vinyl Polysiloxane Impression Material

FDA UDI

Class I (US FDA UDI)

by Dentsply International

Identity

Trade Name
Reprosil® Hydrophilic Vinyl Polysiloxane Impression Material FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Reprosil® VPS Impression Material, Heavy Body (Green), 4 (50ml) Cartridge Refill Package FDA UDI
Model / Reference
626220 FDA UDI
Description
Reprosil® VPS Impression Material, Heavy Body (Green), 4 (50ml) Cartridge Refill Package FDA UDI

Identifiers

Catalog Number
626220 FDA UDI
Primary DI / UDI-DI
D0026262201 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 50 Milliliter FDA UDI

Category: Silicone dental impression material

Reprosil® Hydrophilic Vinyl Polysiloxane Impression Material by Dentsply International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 40d6e4ef-27fc-4a64-b0d0-3cddf950c183 37 fields · synced May 30, 2026