Immco Diagnostics

FDA UDI

Class II (US FDA UDI)

by Immco Diagnostics, Inc.

Identity

Trade Name: IMMCO DIAGNOSTICS FDA UDI
Generic Name: Buffered wash solution IVD, manual FDA UDI
Device Name: WASH BUFFER FDA UDI
Model / Reference: 2308-1 FDA UDI
Description: WASH BUFFER FDA UDI

Identifiers

Catalog Number: 2308-1 FDA UDI
Primary DI / UDI-DI: 00845714004247 FDA UDI
FDA Product Code: MVM FDA UDI
MSV FDA UDI
MST FDA UDI
MOB FDA UDI
LRM FDA UDI
LLL FDA UDI
LJM FDA UDI
DHR FDA UDI
GMDN Term: Buffered wash solution IVD, manual FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 866.5660 FDA UDI
866.5750 FDA UDI
866.5100 FDA UDI
866.5775 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Buffered wash solution IVD, manual

Immco Diagnostics by Immco Diagnostics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Immco Diagnostics, Inc.

Sources (1)

FDA UDI cdc52237-3b22-4082-ba4a-299f611f8f1e 37 fields · synced Sep 17, 2026