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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
Capillary blood collection tube IVD, no additive FDA UDI
Device Name
Capillary tube, end-to-end, 15uL, 20mm long, plain FDA UDI
Model / Reference
172513 FDA UDI
Description
Capillary tube, end-to-end, 15uL, 20mm long, plain FDA UDI

Identifiers

Primary DI / UDI-DI
00840095604420 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Capillary blood collection tube IVD, no additive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6150 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capillary blood collection tube IVD, no additive

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

Similar devices

Also classified as Capillary blood collection tube IVD, no additive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab84b019-dbd0-47f4-87b5-75eecf934d9b 33 fields · synced May 30, 2026