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Acl Top 700

FDA UDI

Class II (US FDA UDI)

by Instrumentation Laboratory Company

Identity

Trade Name
ACL TOP 700 FDA UDI
Generic Name
Coagulation analyser IVD, laboratory FDA UDI
Device Name
ACL TOP 700 (Refurbished) FDA UDI
Model / Reference
00000280010R FDA UDI
Description
ACL TOP 700 (Refurbished) FDA UDI

Identifiers

Catalog Number
00000280010R FDA UDI
Primary DI / UDI-DI
08426950927990 FDA UDI
510(k) Number
K160276 FDA UDI
FDA Product Code
GKP FDA UDI
GMDN Term
Coagulation analyser IVD, laboratory FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5400 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Coagulation analyser IVD, laboratory

Acl Top 700 by Instrumentation Laboratory Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coagulation 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

Sources (1)

  • FDA UDI 2cd343ce-7159-4690-bf9e-117c5fe4f385 36 fields · synced May 30, 2026