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Absolute Pro

FDA UDI

Class III (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
Absolute Pro FDA UDI
Generic Name
Peripheral artery stent, bare-metal FDA UDI
Device Name
Absolute Pro Vascular Self-Expanding Stent System 7.0 mm x 20 mm x 135 cm / Over-The-Wire FDA UDI
Model / Reference
1012535-20 FDA UDI
Description
Absolute Pro Vascular Self-Expanding Stent System 7.0 mm x 20 mm x 135 cm / Over-The-Wire FDA UDI

Identifiers

Catalog Number
1012535-20 FDA UDI
Primary DI / UDI-DI
08717648176043 FDA UDI
FDA Product Code
NIO FDA UDI
GMDN Term
Peripheral artery stent, bare-metal FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
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
MRI Safety
MR Conditional FDA UDI

Category: Peripheral artery stent, bare-metal

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Similar devices

Also classified as Peripheral artery stent, bare-metal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Vascular

Sources (1)

  • FDA UDI 6904828b-2813-432e-b1e0-3c98bec583ea 36 fields · synced Jul 22, 2026