Identity
- Trade Name
- SCANLAN® John Ross Tunneler System FDA UDI
- Generic Name
- Vascular graft tunneller FDA UDI
- Device Name
- SCANLAN® John Ross Tunneler System, 7mm Sheaths FDA UDI
- Model / Reference
- 9009-35 FDA UDI
- Description
- SCANLAN® John Ross Tunneler System, 7mm Sheaths FDA UDI
Identifiers
- Catalog Number
- 9009-35 FDA UDI
- Primary DI / UDI-DI
- 00846159035711 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Vascular graft tunneller FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Vascular graft tunneller
SCANLAN® John Ross Tunneler System by Scanlan International Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Scanlan International Inc
Sources (1)
- FDA UDI 4f46348b-8ed4-4162-9ddc-e1a2f4b317c5 35 fields · synced May 29, 2026