Identity
- Trade Name
- MULTI-LINK VISION FDA UDI
- Generic Name
- Bare-metal coronary artery stent FDA UDI
- Device Name
- MULTI-LINK OTW VISION Coronary Stent System 3.00 mm x 18 mm FDA UDI
- Model / Reference
- 1010143-18 FDA UDI
- Description
- MULTI-LINK OTW VISION Coronary Stent System 3.00 mm x 18 mm FDA UDI
Identifiers
- Catalog Number
- 1010143-18 FDA UDI
- Primary DI / UDI-DI
- 08717648069727 FDA UDI
- FDA Product Code
- MAF FDA UDI
- GMDN Term
- Bare-metal coronary artery stent FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
The MULTI-LINK VISION Coronary Stent System is a non-bioabsorbable, bare-metal tubular device designed to maintain luminal patency and improve luminal diameter in patients with symptomatic atherosclerotic heart disease. Featuring a high-grade stainless steel or cobalt-chrome construction, it may be linear or have a bifurcation design, and is typically balloon-expanded or self-expandable.
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 III | Pending data |
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Manufacturer
- Manufacturer
- Abbott Vascular
Sources (1)
- FDA UDI 9de54e34-bad1-405f-9da2-4b14d029f20f 37 fields · synced Jun 27, 2026