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IMMULITE®/IMMULITE® 1000 Systems DPD Pyrlinks-D

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE®/IMMULITE® 1000 Systems DPD Pyrlinks-D FDA UDI
Generic Name
Collagen pyridium crosslink IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Pyrilinks-D - IMMULITE - RGT - 100 Tests FDA UDI
Model / Reference
10381389 FDA UDI
Description
Pyrilinks-D - IMMULITE - RGT - 100 Tests FDA UDI

Identifiers

Catalog Number
LKPD1 FDA UDI
Primary DI / UDI-DI
00630414964416 FDA UDI
510(k) Number
K980833 FDA UDI
FDA Product Code
JMM FDA UDI
GMDN Term
Collagen pyridium crosslink IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1400 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: Collagen pyridium crosslink IVD, kit, chemiluminescent immunoassay

IMMULITE®/IMMULITE® 1000 Systems DPD Pyrlinks-D by Siemens Healthcare Diagnostics Products Ltd — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Collagen pyridium crosslink 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 63133a7e-7698-4ff2-b02d-9c752cce8b41 37 fields · synced May 30, 2026