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Globe Scientific

FDA UDI

Class II (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 Holding Tray with Sigillum Wax Sealant, 24-Place FDA UDI
Model / Reference
51601 FDA UDI
Description
Capillary Tube Holding Tray with Sigillum Wax Sealant, 24-Place FDA UDI

Identifiers

Primary DI / UDI-DI
00840095607513 FDA UDI
FDA Product Code
GHY FDA UDI
GMDN Term
Capillary blood collection tube IVD, no additive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6400 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 II — 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 555d2eec-bf92-4aae-9965-280a54b4f23f 33 fields · synced May 31, 2026