← Back to catalogue

Globe Scientific

FDA UDI

Class I (US FDA UDI)

by Globe Scientific, Llc

Identity

Trade Name
Globe Scientific FDA UDI
Generic Name
Inoculating tool IVD, manual FDA UDI
Device Name
Inoculation Loop, Rigid, 1uL with Needle, with Calibration Certificate, STERILE, Blue, Individually Wrapped FDA UDI
Model / Reference
2851 FDA UDI
Description
Inoculation Loop, Rigid, 1uL with Needle, with Calibration Certificate, STERILE, Blue, Individually Wrapped FDA UDI

Identifiers

Primary DI / UDI-DI
00840095604673 FDA UDI
FDA Product Code
LIB FDA UDI
GMDN Term
Inoculating tool IVD, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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: Inoculating tool IVD, manual

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

Similar devices

Also classified as Inoculating tool IVD, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 49c80a1f-13f3-4ad9-92d4-24437f09c0a1 33 fields · synced May 30, 2026