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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
Test tube/reservoir cap FDA UDI
Device Name
Cap, Snap, 13mm, PE, for 13mm Glass and Evacuated Tubes and 12mm Plastic Test Tubes, Clear FDA UDI
Model / Reference
113146C FDA UDI
Description
Cap, Snap, 13mm, PE, for 13mm Glass and Evacuated Tubes and 12mm Plastic Test Tubes, Clear FDA UDI

Identifiers

Primary DI / UDI-DI
00840095601900 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Test tube/reservoir cap FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Test tube/reservoir cap

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

Similar devices

Also classified as Test tube/reservoir cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0212652e-b120-4709-b197-1a0a3f70be86 33 fields · synced May 30, 2026