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Vp2000

FDA UDI

Class I (US FDA UDI)

by Abbott Molecular

Identity

Trade Name
VP2000 FDA UDI
Generic Name
Tissue processor IVD, automated/semi-automated FDA UDI
Device Name
Abbott VP2000 Processor Operations Manual, Rev. D FDA UDI
Model / Reference
03N27-51 FDA UDI
Description
Abbott VP2000 Processor Operations Manual, Rev. D FDA UDI

Identifiers

Catalog Number
03N27-51 FDA UDI
Primary DI / UDI-DI
00884999037595 FDA UDI
FDA Product Code
KEY FDA UDI
GMDN Term
Tissue processor IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3800 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue processor IVD, automated/semi-automated

Vp2000 by Abbott Molecular — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue processor IVD, automated/semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Molecular

Sources (1)

  • FDA UDI 4e51dcb0-a16a-4917-9e12-1097058eac0b 35 fields · synced Jun 1, 2026