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NoCord VPS

FDA UDI

Class U (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
NoCord VPS FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
NoCord VPS Retraction Wash impression material, 10 pk FDA UDI
Model / Reference
310284 FDA UDI
Description
NoCord VPS Retraction Wash impression material, 10 pk FDA UDI

Identifiers

Primary DI / UDI-DI
00817051020808 FDA UDI
FDA Product Code
MVL FDA UDI
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Category: Silicone dental impression material

NoCord VPS by Centrix, Inc. — Class U — 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

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI 2056b722-33b0-466b-93e3-d25771dd8bb0 33 fields · synced May 30, 2026