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m2000

FDA UDI

Class I (US FDA UDI)

by Abbott Molecular

Identity

Trade Name
m2000 FDA UDI
Generic Name
Instrument/analyser specimen/reagent container carrier IVD FDA UDI
Device Name
Splash Free Support Base FDA UDI
Model / Reference
9K31-01 FDA UDI
Description
Splash Free Support Base FDA UDI

Identifiers

Catalog Number
9K31-01 FDA UDI
Primary DI / UDI-DI
00884999032057 FDA UDI
510(k) Number
K092705 FDA UDI
FDA Product Code
JJH FDA UDI
OOI FDA UDI
GMDN Term
Instrument/analyser specimen/reagent container carrier IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 FDA UDI
862.2570 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument/analyser specimen/reagent container carrier IVD

m2000 by Abbott Molecular — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/analyser specimen/reagent container carrier IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Molecular

Sources (1)

  • FDA UDI a2a558a5-abdf-428c-9b42-b0e45769fb38 36 fields · synced Jun 1, 2026