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IMMULITE® 2000 Systems PHE Phenobarbital

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE® 2000 Systems PHE Phenobarbital FDA UDI
Generic Name
Phenobarbital therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Phenobarbital - IMMULITE - RGT - 200 Tests FDA UDI
Model / Reference
10381542 FDA UDI
Description
Phenobarbital - IMMULITE - RGT - 200 Tests FDA UDI

Identifiers

Catalog Number
L2KPB2 FDA UDI
Primary DI / UDI-DI
00630414961828 FDA UDI
510(k) Number
K970227 FDA UDI
FDA Product Code
DLZ FDA UDI
GMDN Term
Phenobarbital therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3660 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phenobarbital therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay

IMMULITE® 2000 Systems PHE Phenobarbital by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Phenobarbital therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay.

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 b06575d0-a653-4059-bcd1-20c33ce43162 37 fields · synced Jun 8, 2026