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LAtrol ABNORMAL CONTROL PLASMA

FDA UDI

Class II (US FDA UDI)

by Biomedica ADI Inc.

Identity

Trade Name
LAtrol ABNORMAL CONTROL PLASMA FDA UDI
Generic Name
Lupus anticoagulant marker IVD, control FDA UDI
Model / Reference
816A FDA UDI

Identifiers

Catalog Number
816A FDA UDI
Primary DI / UDI-DI
00850201006130 FDA UDI
FDA Product Code
GGC FDA UDI
GMDN Term
Lupus anticoagulant marker IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5425 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

Yes

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

No

FDA UDI

Category: Lupus anticoagulant marker IVD, control

LAtrol ABNORMAL CONTROL PLASMA by Biomedica ADI Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lupus anticoagulant marker IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomedica ADI Inc.

Sources (1)

  • FDA UDI 7b74507d-8379-41ec-8fa2-a9de6d517527 33 fields · synced May 30, 2026