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IMMULITE® Systems PTH Calibration Verification Material Intact PTH

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE® Systems PTH Calibration Verification Material Intact PTH FDA UDI
Generic Name
Parathyroid hormone (PTH) IVD, control FDA UDI
Device Name
PTH Intact CVM - IMMULITE - CONS FDA UDI
Model / Reference
10388105 FDA UDI
Description
PTH Intact CVM - IMMULITE - CONS FDA UDI

Identifiers

Catalog Number
LPPCVM FDA UDI
Primary DI / UDI-DI
00630414979410 FDA UDI
510(k) Number
K020217 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Parathyroid hormone (PTH) IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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, control

IMMULITE® Systems PTH Calibration Verification Material Intact PTH by Siemens Healthcare Diagnostics Products Ltd — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Parathyroid hormone (PTH) IVD, control.

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 ceed7bc2-afa4-42d5-83fb-bd35f31bcf77 37 fields · synced Jun 8, 2026