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SCANLAN® Aorta Vein Punch
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 1001-04ARef 1001-06Ref 1001-03Ref 1001-04
Identity
- Trade Name
- SCANLAN® Aorta Vein Punch FDA UDI
- Generic Name
- Aorta punch, single-use FDA UDI
- Device Name
- SCANLAN® Aorta/Vein Punch EUDAMEDAorta Vein Punch with Sterilizing Tray FDA UDIAorta Vein Punch FDA UDI
- Model / Reference
- 1001-04 EUDAMEDFDA UDI1001-04A EUDAMEDFDA UDI1001-03 EUDAMEDFDA UDI1001-06 EUDAMEDFDA UDI
- Description
- Aorta Vein Punch with Sterilizing Tray FDA UDIAorta Vein Punch FDA UDI
Identifiers
- Catalog Number
- 1001-04 FDA UDI1001-04A FDA UDI1001-03 FDA UDI1001-06 FDA UDI
- Primary DI / UDI-DI
- 00846159007275 EUDAMEDFDA UDI00846159007282 EUDAMEDFDA UDI00846159027044 EUDAMEDFDA UDI00846159007329 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00846159007282 EUDAMEDB-00846159007329 EUDAMEDB-00846159027044 EUDAMEDB-00846159007275 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 (8)
- FDA UDI acd0e4ea-cde3-4cf9-9dc0-5d53487d4c6e 35 fields · synced Jul 18, 2026
- FDA UDI d0ea78e6-40cf-46d4-aa3e-e1a5d69df7d2 35 fields · synced May 29, 2026
- FDA UDI 17ae50ac-2462-4698-b326-35e0c2827b80 35 fields · synced May 30, 2026
- FDA UDI a04e3fb2-95cc-4ac5-9f01-bff64f327fac 35 fields · synced May 30, 2026
- EUDAMED 02674d8c-131b-4174-bd3c-9dcb9a5a22b4 61 fields · synced Jul 9, 2026
- EUDAMED 3595a09f-148b-4e46-a1ce-9bc3f381721b 61 fields · synced Jul 13, 2026
- EUDAMED 75003c03-a11e-4a0e-b282-ac5a4fac4dd3 61 fields · synced Jul 17, 2026
- EUDAMED 5418c897-0bd1-4b7c-af3f-795def2982c0 61 fields · synced Jul 18, 2026