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Vivid Alginate Substitute Std Pkg

FDA UDI

Class II (US FDA UDI)

by Pearson Dental Supplies, Inc.

Identity

Trade Name
Vivid Alginate Substitute Std Pkg FDA UDI
Generic Name
Polysulfide dental impression material FDA UDI
Model / Reference
B31-0021 FDA UDI

Identifiers

Primary DI / UDI-DI
D724B3100211 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Polysulfide 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

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

Yes

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: Polysulfide dental impression material

Vivid Alginate Substitute Std Pkg by Pearson Dental Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polysulfide dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f8864114-e3d0-4c04-8ead-ca6009894168 32 fields · synced Jun 8, 2026