Identity
- Trade Name
- EU Retrax Gel AS Micropoint Kits EUDAMEDEU Retrax Gel AS MicroPoints FDA UDI
- Generic Name
- Gingival retraction solution FDA UDI
- Device Name
- Retrax Gel AS EUDAMEDTopical Hemostatic 25% aluminum sulfate gel - 25 - 0.32g MicroPoint Cartridges. FDA UDI
- Model / Reference
- 16505 EUDAMEDFDA UDI
- Description
- Topical Hemostatic 25% aluminum sulfate gel - 25 - 0.32g MicroPoint Cartridges. FDA UDI
Identifiers
- Catalog Number
- 16505 FDA UDI
- Primary DI / UDI-DI
- 00310866002262 EUDAMEDFDA UDI
- Basic UDI-DI
- 03108665001GK 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 EUDAMEDU FDA UDI
- Market of Registration
- Austria 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 — 0.32 Gram FDA UDI
EU Retrax Gel AS Micropoint Kits by Pascal Company, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 03108665001GK | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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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 f75ecc1e-97f9-4205-9b43-099ebcb21de1 61 fields · synced Aug 3, 2026
- FDA UDI c5eaa327-fc29-4ddf-b2ef-e70246ea4608 37 fields · synced May 30, 2026