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Advanced Instruments GloCyte® Test Cartridge Kit - 8 Trays

FDA UDI

Class II (US FDA UDI)

by Advanced Instruments, LLC

Identity

Trade Name
Advanced Instruments GloCyte® Test Cartridge Kit - 8 Trays FDA UDI
Generic Name
Haematological cell analyser IVD FDA UDI
Device Name
For In Vitro Diagnostic Use. Advanced Instruments GloCyte® Test Cartridge Kit - 8 Trays has been developed for use exclusively with the Advanced Instruments GloCyte® Automated Cell Counter System. Contains 200 test cartridges. FDA UDI
Model / Reference
111010 FDA UDI
Description
For In Vitro Diagnostic Use. Advanced Instruments GloCyte® Test Cartridge Kit - 8 Trays has been developed for use exclusively with the Advanced Instruments GloCyte® Automated Cell Counter System. Contains 200 test cartridges. FDA UDI

Identifiers

Catalog Number
111010 FDA UDI
Primary DI / UDI-DI
20816068020201 FDA UDI
510(k) Number
K152776 FDA UDI
FDA Product Code
GKL FDA UDI
GMDN Term
Haematological cell analyser IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5200 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haematological cell analyser IVD

Advanced Instruments GloCyte® Test Cartridge Kit - 8 Trays by Advanced Instruments, LLC — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Haematological cell analyser IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 112266c7-9dd2-4115-b843-b3600ff350d2 37 fields · synced Jun 8, 2026