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Retrax Gel AS Clear Pro Pack

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 16840

by Pascal Company Inc.

Identity

Trade Name
Retrax Gel AS Clear Pro Pack EUDAMED
EU Retrax Gel AS Clear ProPack FDA UDI
Generic Name
Gingival retraction solution FDA UDI
Device Name
Retrax Gel FS EUDAMED
25% aluminum sulfate gel, 12 - 0.75g syringe; no color FDA UDI
Model / Reference
16840 EUDAMEDFDA UDI
Description
25% aluminum sulfate gel, 12 - 0.75g syringe; no color FDA UDI

Identifiers

Catalog Number
16840 FDA UDI
Primary DI / UDI-DI
00310866002330 EUDAMEDFDA UDI
Basic UDI-DI
03108665004GR EUDAMED
FDA Product Code
MVL FDA UDI
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED
GMDN Term
Gingival retraction solution FDA UDI

Classification

Device Class
Class I EUDAMED
U FDA UDI
Market of Registration
Romania EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 cord, non-medicated

Retrax Gel AS Clear Pro Pack by Pascal Company, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pascal Company Inc.
EUDAMED SRN
US-MF-000032036
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED a129defe-ef52-403b-bf1d-205c45b8026c 61 fields · synced Jul 21, 2026
  • FDA UDI 89620e03-e658-46e3-b934-8d80f5af4ca4 37 fields · synced May 30, 2026