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Leica Biosystems CytoVision GSL WinXP-&gt +1 more model

FDA UDI

Class II (US FDA UDI)

by Leica Biosystems Richmond, Inc.

Identity

Trade Name
Leica Biosystems CytoVision GSL WinXP->Win7 with current CV version FDA UDI
Generic Name
Laboratory instrument/analyser application software IVD FDA UDI
Device Name
Leica Biosystems CytoVision GSL WinXP->Win7 with current CV version FDA UDI
Model / Reference
23GSLXXXKFXUPG FDA UDI
Description
Leica Biosystems CytoVision GSL WinXP->Win7 with current CV version FDA UDI

Identifiers

Primary DI / UDI-DI
00849832003762 FDA UDI
FDA Product Code
JOY FDA UDI
GMDN Term
Laboratory instrument/analyser application software IVD FDA UDI
Models / Variants
Leica Biosystems CytoVision GSL WinXP-&gt FDA UDI
Win7 with current CV version FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5260 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Leica Biosystems CytoVision GSL WinXP-&gt +1 more model by Leica Biosystems Richmond, Inc. — Class II — FDA UDI — listed in FDA GUDID — 2 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Leica Biosystems Richmond, Inc.

Sources (1)

  • FDA UDI 3cb06043-6925-4668-a3ca-f2b687ad5633 37 fields · synced May 31, 2026