← 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
General specimen microscopy slide IVD, single-use FDA UDI
Device Name
Diagnostic microscope slide, Black Epoxy Ink, 10 well, 6 mm, 10mm Frosted end FDA UDI
Model / Reference
1398-106K-10 FDA UDI
Description
Diagnostic microscope slide, Black Epoxy Ink, 10 well, 6 mm, 10mm Frosted end FDA UDI

Identifiers

Primary DI / UDI-DI
00840095686037 FDA UDI
FDA Product Code
KEW FDA UDI
GMDN Term
General specimen microscopy slide IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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: General specimen microscopy slide IVD, single-use

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

Similar devices

Also classified as General specimen microscopy slide IVD, single-use.

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 00278f6b-2d33-4eb6-b660-0cee4fa56c44 33 fields · synced May 29, 2026