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Prestige Hydrolight 2 X 50 Ml

FDA UDI

Class II (US FDA UDI)

by Vannini Dental Industry Srl

Identity

Trade Name
PRESTIGE HYDROLIGHT 2 X 50 ML FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Vinylpolisiloxane for impressions FDA UDI
Model / Reference
055250 FDA UDI
Description
Vinylpolisiloxane for impressions FDA UDI

Identifiers

Catalog Number
055250 FDA UDI
Primary DI / UDI-DI
08033712562186 FDA UDI
510(k) Number
K083739 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Total Volume — 100 Milliliter FDA UDI

Category: Silicone dental impression material

Prestige Hydrolight 2 X 50 Ml by Vannini Dental Industry Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c6cbeb7-d306-46ae-b3d9-ff2db3b67f53 38 fields · synced Jun 8, 2026