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TiMO™ Tube Management Holder

FDA UDI

Class I (US FDA UDI)

by Itl Asia Pacific Sdn. Bhd.

Identity

Trade Name
TiMO™ Tube Management Holder FDA UDI
Generic Name
Instrument/analyser specimen/reagent container carrier IVD FDA UDI
Device Name
TiMO™ is intended as a sample test tube holder to assist with the management of the sample tubes during blood collection. FDA UDI
Model / Reference
C100400 FDA UDI
Description
TiMO™ is intended as a sample test tube holder to assist with the management of the sample tubes during blood collection. FDA UDI

Identifiers

Primary DI / UDI-DI
19555240400083 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Instrument/analyser specimen/reagent container carrier IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument/analyser specimen/reagent container carrier IVD

TiMO™ Tube Management Holder by Itl Asia Pacific Sdn. Bhd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/analyser specimen/reagent container carrier IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Itl Asia Pacific Sdn. Bhd.

Sources (1)

  • FDA UDI 4a7d8566-a7e1-4d56-b3b4-94022873e764 34 fields · synced May 30, 2026