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Disposet
EUDAMEDClass IIa (EU MDR)
Ref 959-511007-000
by Di̇sposet Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇
Identity
- Trade Name
- Disposet EUDAMED
- Device Name
- Aortic Punch EUDAMED
- Model / Reference
- 959-511007-000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08681049566942 EUDAMED
- Basic UDI-DI
- B-08681049566942 EUDAMED
- EMDN Code
- C01901201 AORTIC PUNCHES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Türkiye EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Category: Aorta punch, single-use
Disposet by Di̇sposet Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Aorta punch, single-use.
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- SCANLAN® A/V Punch — SCANLAN INTERNATIONAL INC · Class I
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08681049566942 | Class IIa | Active |
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Manufacturer
- EUDAMED SRN
- TR-MF-000018945
Sources (1)
- EUDAMED 3c1d942b-a9d7-447b-a6cb-aff4e8706e15 61 fields · synced Jun 18, 2026