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Cell-Dyn

FDA UDI

Class II (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
CELL-DYN FDA UDI
Generic Name
Full blood count IVD, control FDA UDI
Device Name
CELL-DYN 18 PLUS CONTROL FDA UDI
Model / Reference
09H69-01 FDA UDI
Description
CELL-DYN 18 PLUS CONTROL FDA UDI

Identifiers

Catalog Number
09H6901 FDA UDI
Primary DI / UDI-DI
00380740020323 FDA UDI
510(k) Number
K823498 FDA UDI
FDA Product Code
GLQ FDA UDI
GMDN Term
Full blood count IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.8625 FDA UDI
Commercial Distribution
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

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: Full blood count IVD, control

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

Similar devices

Also classified as Full blood count IVD, control.

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 99b7aa10-bd08-4d10-a488-08f773cd4f67 37 fields · synced May 30, 2026