← Back to catalogue

Lactate Plus

FDA UDI

Class I (US FDA UDI)

by Nova Biomedical Corporation

Identity

Trade Name
Lactate Plus FDA UDI
Generic Name
Lactate IVD, control FDA UDI
Device Name
Lactate Plus LAC Control 1 FDA UDI
Model / Reference
Lactate Plus FDA UDI
Description
Lactate Plus LAC Control 1 FDA UDI

Identifiers

Catalog Number
40815 FDA UDI
Primary DI / UDI-DI
00385480408158 FDA UDI
FDA Product Code
KHP FDA UDI
GMDN Term
Lactate IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1450 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Lactate IVD, control

Lactate Plus by Nova Biomedical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lactate IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c59997a6-2925-4130-ac11-f4ccffaffbe1 36 fields · synced Jun 8, 2026