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iTrac

FDA UDI

Class I (US FDA UDI)

by Pivotal Health Solutions

Identity

Trade Name
iTrac FDA UDI
Generic Name
Traction table, line-powered FDA UDI
Device Name
iTrac, 230V FDA UDI
Model / Reference
T9010 FDA UDI
Description
iTrac, 230V FDA UDI

Identifiers

Primary DI / UDI-DI
00852753008952 FDA UDI
FDA Product Code
ILZ FDA UDI
IRS FDA UDI
ITH FDA UDI
GMDN Term
Traction table, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5925 FDA UDI
890.5900 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Traction table, line-powered

iTrac by Pivotal Health Solutions — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Traction table, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 84ea619b-9b91-4e90-8c84-b6e9c41bbaa4 33 fields · synced Jun 9, 2026