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Bosworth

FDA UDI

Class II (US FDA UDI)

by Harry J. Bosworth Co.

Identity

Trade Name
Bosworth FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Standard 37% Etch Gel Kit FDA UDI
Model / Reference
0921346 FDA UDI
Description
Standard 37% Etch Gel Kit FDA UDI

Identifiers

Catalog Number
0921346 FDA UDI
Primary DI / UDI-DI
H66809213461 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

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 — 3 Milliliter FDA UDI

Category: Dental etching solution

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

Similar devices

Also classified as Dental etching solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a56491f2-07d7-4b0f-ac40-7e66cfe46a33 37 fields · synced May 30, 2026