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Reticcount

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
Reticcount FDA UDI
Generic Name
Reticulocyte count IVD, reagent FDA UDI
Device Name
Retic-Count Reticulocyte Rgnt System IVD FDA UDI
Model / Reference
349204 FDA UDI
Description
Retic-Count Reticulocyte Rgnt System IVD FDA UDI

Identifiers

Catalog Number
349204 FDA UDI
Primary DI / UDI-DI
00382903492046 FDA UDI
FDA Product Code
GKL FDA UDI
GMDN Term
Reticulocyte count IVD, reagent 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Reticulocyte count IVD, reagent

Reticcount by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reticulocyte count IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cd3c1d4a-a984-4bd7-b444-438f4e1e72c0 36 fields · synced Jun 8, 2026