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Cell-Dyn

FDA UDI

Class I (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
CELL-DYN FDA UDI
Generic Name
Blood cell lysis reagent IVD FDA UDI
Device Name
CELL-DYN 1800 System CN-FREE DIFF LYSE FDA UDI
Model / Reference
07H84-01 FDA UDI
Description
CELL-DYN 1800 System CN-FREE DIFF LYSE FDA UDI

Identifiers

Catalog Number
07H8401 FDA UDI
Primary DI / UDI-DI
00380740013547 FDA UDI
FDA Product Code
GGK FDA UDI
GMDN Term
Blood cell lysis reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.8540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Cell-Dyn by Abbott Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a0009e6b-2b49-40e7-8fa8-18d061be8ac1 36 fields · synced May 31, 2026