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Barrier Gel

FDA UDI

Class II (US FDA UDI)

by Bisco Inc.

Identity

Trade Name
Barrier Gel FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Barrier Gel 5g Syringe FDA UDI
Model / Reference
G-9602 FDA UDI
Description
Barrier Gel 5g Syringe FDA UDI

Identifiers

Catalog Number
G-9602 FDA UDI
Primary DI / UDI-DI
00810111542012 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 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

Category: Dental etching solution

Barrier Gel by Bisco Inc. — 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

Manufacturer
Bisco Inc.

Sources (1)

  • FDA UDI 84cb7488-7a58-443e-b66e-1153274c5afc 36 fields · synced May 30, 2026