← Back to catalogue

Immco Diagnostics

FDA UDI

Class II (US FDA UDI)

by Immco Diagnostics, Inc.

Identity

Trade Name
IMMCO DIAGNOSTICS FDA UDI
Generic Name
Buffered sample diluent IVD, manual FDA UDI
Device Name
Serum Diluent FDA UDI
Model / Reference
5305 FDA UDI
Description
Serum Diluent FDA UDI

Identifiers

Catalog Number
5305 FDA UDI
Primary DI / UDI-DI
00845714002953 FDA UDI
FDA Product Code
MID FDA UDI
GMDN Term
Buffered sample diluent IVD, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5660 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

Yes

FDA UDI

Category: Buffered sample diluent IVD, manual

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

Similar devices

Also classified as Buffered sample diluent IVD, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Immco Diagnostics, Inc.

Sources (1)

  • FDA UDI c4e7de00-5cc3-4f04-8fc2-02d5fb2c4df1 37 fields · synced Sep 17, 2026