Identity
- Trade Name
- SCANLAN® Aorta Vein Punch FDA UDI
- Generic Name
- Aorta punch, single-use FDA UDI
- Device Name
- SCANLAN® Aorta/Vein Punch Sterilizing Box and Tray EUDAMEDAorta Vein Punch with Sterilizing Tray FDA UDI
- Model / Reference
- 1001-05 EUDAMEDFDA UDI
- Description
- Aorta Vein Punch with Sterilizing Tray FDA UDI
Identifiers
- Catalog Number
- 1001-05 FDA UDI
- Primary DI / UDI-DI
- 00846159007305 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00846159007305 EUDAMED
- FDA Product Code
- DWS FDA UDI
- EMDN Code
- L01040402 VASCULAR SCISSORS, REUSABLE EUDAMED
- GMDN Term
- Aorta punch, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 870.4500 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Aorta punch, single-use
SCANLAN® Aorta Vein Punch by Scanlan International Inc — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Aorta punch, single-use.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Scanlan International Inc
Sources (2)
- FDA UDI 64e92121-38c0-4df3-a7fb-0ae877247ed7 35 fields · synced Jun 18, 2026
- EUDAMED 5b39500b-c48f-4b11-9159-0b25dd58238b 61 fields · synced Jun 18, 2026