Ultraflo-T

FDA UDI

Class I (US FDA UDI)

by Innovative Medical Technologies, Inc.

Identity

Trade Name: ULTRAFLO-T FDA UDI
Generic Name: Syringe/blood collection tube adaptor IVD FDA UDI
Device Name: FEMALE LUER BLOOD TRANSFER DEVICE FDA UDI
Model / Reference: 810 FDA UDI
Description: FEMALE LUER BLOOD TRANSFER DEVICE FDA UDI

Identifiers

Catalog Number: 810 FDA UDI
Primary DI / UDI-DI: 20857182006283 FDA UDI
FDA Product Code: KST FDA UDI
GMDN Term: Syringe/blood collection tube adaptor IVD FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 864.9125 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Syringe/blood collection tube adaptor IVD

Ultraflo-T by Innovative Medical Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Syringe/blood collection tube adaptor IVD.

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Vacuette — Greiner Bio-One GmbH · Class I
BD Vacutainer® Blood Transfer Device Holder — BECTON DICKINSON AND COMPANY · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Innovative Medical Technologies, Inc.

Sources (1)

FDA UDI d7c00b88-dd16-4c4a-a851-811e91205c56 35 fields · synced Jun 8, 2026