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Hi-Torque Command

FDA UDI

Class II (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
HI-TORQUE COMMAND FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
Hi-Torque Command 18 ST Guide Wire .018" 10 cm / 4 g, 300 cm FDA UDI
Model / Reference
1013731 FDA UDI
Description
Hi-Torque Command 18 ST Guide Wire .018" 10 cm / 4 g, 300 cm FDA UDI

Identifiers

Catalog Number
1013731 FDA UDI
Primary DI / UDI-DI
08717648212130 FDA UDI
FDA Product Code
DQX FDA UDI
GMDN Term
Peripheral vascular guidewire, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral vascular guidewire, manual

Hi-Torque Command by Abbott Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular guidewire, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Vascular

Sources (1)

  • FDA UDI 0f0574d8-2210-4289-acdd-5e3aeb87458c 36 fields · synced May 31, 2026