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L.pneuGR1-6&Mic.Screen(HT)18W

FDA UDI

Class II (US FDA UDI)

by Scimedx Corp.

Identity

Trade Name
L.pneuGR1-6&Mic.Screen(HT)18W FDA UDI
Generic Name
Legionella pneumophila total antibody IVD, kit, fluorescent immunoassay FDA UDI
Model / Reference
CLEGMIC FDA UDI

Identifiers

Catalog Number
CLEGMIC FDA UDI
Primary DI / UDI-DI
00813545025014 FDA UDI
FDA Product Code
LHL FDA UDI
GMDN Term
Legionella pneumophila total antibody IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3300 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Legionella pneumophila total antibody IVD, kit, fluorescent immunoassay

L.pneuGR1-6&Mic.Screen(HT)18W by Scimedx Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Legionella pneumophila total antibody IVD, kit, fluorescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scimedx Corp.

Sources (1)

  • FDA UDI 33293a5e-3848-4709-93ea-6004ba81c968 34 fields · synced May 30, 2026