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EU Retrax Gel AS ProPack Sample

FDA UDIEUDAMED

Class U (US FDA UDI)

by Pascal Company, Inc.

Identity

Trade Name
EU Retrax Gel AS ProPack Sample FDA UDI
Generic Name
Gingival retraction solution FDA UDI
Device Name
25% aluminum sulfate gel, 2 - .75g syringe; Green FDA UDI
Model / Reference
88102 FDA UDI
Description
25% aluminum sulfate gel, 2 - .75g syringe; Green FDA UDI

Identifiers

Catalog Number
88102 FDA UDI
Primary DI / UDI-DI
00310866002378 FDA UDI
FDA Product Code
MVL FDA UDI
GMDN Term
Gingival retraction solution FDA UDI

Classification

Device Class
U 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

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 — 0.75 Gram FDA UDI

Category: Gingival retraction solution

EU Retrax Gel AS ProPack Sample by Pascal Company, Inc. — Class U — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction solution.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 98d1a251-5b2a-4c8d-a9e8-cc760f973841 37 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026