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Retrax Gel AS Jar

FDA UDI

Class U (US FDA UDI)

by Pascal Company, Inc.

Identity

Trade Name
Retrax Gel AS Jar FDA UDI
Generic Name
Gingival retraction kit FDA UDI
Device Name
Topical Hemostatic Gel 30g Jar 25% aluminum sulfate gel 30g jar; Green FDA UDI
Model / Reference
15510 FDA UDI
Description
Topical Hemostatic Gel 30g Jar 25% aluminum sulfate gel 30g jar; Green FDA UDI

Identifiers

Catalog Number
15510 FDA UDI
Primary DI / UDI-DI
00310866002309 FDA UDI
FDA Product Code
MVL FDA UDI
GMDN Term
Gingival retraction kit FDA UDI

Classification

Device Class
U 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

Category: Gingival retraction kit

Retrax Gel AS Jar by Pascal Company, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c4fee41-c492-4c00-9c55-70c8c8166799 36 fields · synced May 29, 2026