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Ultraflo-V

FDA UDI

Class II (US FDA UDI)

by Innovative Medical Technologies, Inc.

Identity

Trade Name
ULTRAFLO-V FDA UDI
Generic Name
Blood collection tube holder/needle FDA UDI
Device Name
SAFETY BLOOD COLLECTION SET 22GX1.25" FDA UDI
Model / Reference
608 FDA UDI
Description
SAFETY BLOOD COLLECTION SET 22GX1.25" FDA UDI

Identifiers

Catalog Number
608 FDA UDI
Primary DI / UDI-DI
10857182006224 FDA UDI
510(k) Number
K172763 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Blood collection tube holder/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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: Blood collection tube holder/needle

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

Similar devices

Also classified as Blood collection tube holder/needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 69bb978b-0bd7-4982-b0fd-00e77e1fd11a 36 fields · synced May 30, 2026