← Back to catalogue

IMMULITE® 2000 Systems IPT Intact PTH

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE® 2000 Systems IPT Intact PTH FDA UDI
Generic Name
Parathyroid hormone (PTH) IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
PTH intact - IMMULITE - RGT - 200 Tests FDA UDI
Model / Reference
10381441 FDA UDI
Description
PTH intact - IMMULITE - RGT - 200 Tests FDA UDI

Identifiers

Catalog Number
L2KPP2 FDA UDI
Primary DI / UDI-DI
00630414961910 FDA UDI
510(k) Number
K013566 FDA UDI
FDA Product Code
CEW FDA UDI
GMDN Term
Parathyroid hormone (PTH) IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1545 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: Parathyroid hormone (PTH) IVD, kit, chemiluminescent immunoassay

IMMULITE® 2000 Systems IPT Intact PTH by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Parathyroid hormone (PTH) IVD, kit, chemiluminescent immunoassay.

Cleared under the same submission

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 7f4ce9a7-c4f3-4bd2-a758-6eb054e43711 37 fields · synced Jun 8, 2026