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Universalcont.25ml W/Screw &label Si

FDA UDI

Class I (US FDA UDI)

by Nunc A/S

Identity

Trade Name
UNIVERSALCONT.25ML W/SCREW &LABEL SI FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
UNIVERSALCONT 25ML W/SCREWC &LABEL SI FDA UDI
Model / Reference
364246 FDA UDI
Description
UNIVERSALCONT 25ML W/SCREWC &LABEL SI FDA UDI

Identifiers

Primary DI / UDI-DI
15713311000110 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Blood/tissue storage/culture container

Universalcont.25ml W/Screw &label Si by Nunc A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood/tissue storage/culture container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nunc A/S

Sources (1)

  • FDA UDI 8762b0c3-a492-4df4-96cd-ca69c4f09d9f 33 fields · synced May 30, 2026