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Isi

FDA UDI

Class I (US FDA UDI)

by Instrument Specialists, Inc.

Identity

Trade Name
ISI FDA UDI
Generic Name
Upper-limb traction wrap/trap, reusable FDA UDI
Device Name
Traction Strap FDA UDI
Model / Reference
Traction Strap FDA UDI
Description
Traction Strap FDA UDI

Identifiers

Catalog Number
WS1820 FDA UDI
Primary DI / UDI-DI
00810045920566 FDA UDI
FDA Product Code
ILZ FDA UDI
GMDN Term
Upper-limb traction wrap/trap, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5925 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Upper-limb traction wrap/trap, reusable

Isi by Instrument Specialists, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Upper-limb traction wrap/trap, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 755e7b58-8f38-4405-bf71-114fddb895ff 34 fields · synced May 29, 2026