Identity
- Trade Name
- Paramount EUDAMED
- Device Name
- Dermal Curette EUDAMED
- Model / Reference
- 2.0, 3.0, 4.0, 5.0, 7.0 mm EUDAMEDDCS7.0 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08903175003048 EUDAMED
- Basic UDI-DI
- 8903175PSLDC65 EUDAMED
- EMDN Code
- A01020303 CUTANEOUS BIOPSY CURETTES, SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
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
Category: Dermal curette, single-use
Paramount by Paramount Surgimed Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Dermal curette, single-use.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8903175PSLDC65 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Paramount Surgimed Limited
- EUDAMED SRN
- IN-MF-000021682
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (1)
- EUDAMED 9eaa64f4-00eb-4bea-b376-46882f83d480 61 fields · synced Jun 17, 2026