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Dimension® PALB Calibrator

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension® PALB Calibrator FDA UDI
Generic Name
Prealbumin (transthyretin) IVD, calibrator FDA UDI
Device Name
Prealbumin Calibrator, 2x5x1mL FDA UDI
Model / Reference
10445025 FDA UDI
Description
Prealbumin Calibrator, 2x5x1mL FDA UDI

Identifiers

Catalog Number
DC50 FDA UDI
Primary DI / UDI-DI
00842768005183 FDA UDI
510(k) Number
K982292 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
Prealbumin (transthyretin) IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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: Prealbumin (transthyretin) IVD, calibrator

Dimension® PALB Calibrator by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Prealbumin (transthyretin) IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 29a89787-309b-4d18-a706-1fc0d807b67d 37 fields · synced Jun 1, 2026