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Abx Pentra 400 Ise

FDA UDI

Class I (US FDA UDI)

by Horiba Abx

Identity

Trade Name
ABX PENTRA 400 ISE FDA UDI
Generic Name
Multiple clinical chemistry analyser IVD, laboratory FDA UDI
Device Name
ABX PENTRA 400 ISE (OCCASION) FDA UDI
Model / Reference
1280030035 FDA UDI
Description
ABX PENTRA 400 ISE (OCCASION) FDA UDI

Identifiers

Primary DI / UDI-DI
03610230005880 FDA UDI
510(k) Number
K052007 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Multiple clinical chemistry analyser IVD, laboratory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple clinical chemistry analyser IVD, laboratory

Abx Pentra 400 Ise by Horiba Abx — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple clinical chemistry analyser IVD, laboratory.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Horiba Abx

Sources (1)

  • FDA UDI 58982052-3234-41c9-8a0b-7a41ca0fe730 34 fields · synced Jun 8, 2026