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Globe Scientific

FDA UDI

Class I (US FDA UDI)

by Globe Scientific, Llc

Identity

Trade Name
Globe Scientific FDA UDI
Generic Name
Microbial cryotube IVD FDA UDI
Device Name
CryoCLEAR vials, 2.0mL, STERILE, External Threads, Assembled BLUE Screwcap with Co-Molded Thermoplastic Elastomer (TPE) Sealing Layer, Round Bottom, Self-Standing, Printed Graduations, Writing Space and Barcode, 50/Bag, 10 Bags/Case FDA UDI
Model / Reference
3012B FDA UDI
Description
CryoCLEAR vials, 2.0mL, STERILE, External Threads, Assembled BLUE Screwcap with Co-Molded Thermoplastic Elastomer (TPE) Sealing Layer, Round Bottom, Self-Standing, Printed Graduations, Writing Space and Barcode, 50/Bag, 10 Bags/Case FDA UDI

Identifiers

Primary DI / UDI-DI
00840095646253 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
Microbial cryotube IVD 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microbial cryotube IVD

Globe Scientific by Globe Scientific, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microbial cryotube IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Globe Scientific, Llc

Sources (1)

  • FDA UDI 58142fd8-f045-41de-9fa2-4c2a7af3c89e 33 fields · synced Jun 6, 2026