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Bosworth Supergel

FDA UDI

Class II (US FDA UDI)

by Harry J. Bosworth Co.

Identity

Trade Name
Bosworth Supergel FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
Alginate Impression Pwd 25 lb Fast Set FDA UDI
Model / Reference
0921831 FDA UDI
Description
Alginate Impression Pwd 25 lb Fast Set FDA UDI

Identifiers

Catalog Number
09218312 FDA UDI
Primary DI / UDI-DI
H66809218321 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Alginate 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

Yes

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
Weight — 25 Pound FDA UDI
Weight — 11.34 Kilogram FDA UDI

Category: Alginate dental impression material

Bosworth Supergel by Harry J. Bosworth Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alginate dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 13196ed6-123f-45a8-8950-e7552e26fa70 37 fields · synced May 30, 2026