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Architect

FDA UDI

Class II (US FDA UDI)

by Abbott

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Parathyroid hormone (PTH) IVD, calibrator FDA UDI
Device Name
ARCHITECT Intact PTH Calibrators FDA UDI
Model / Reference
08K2504 FDA UDI
Description
ARCHITECT Intact PTH Calibrators FDA UDI

Identifiers

Catalog Number
08K2504 FDA UDI
Primary DI / UDI-DI
00380740156039 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
Parathyroid hormone (PTH) 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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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, calibrator

Architect by Abbott — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI 9365d335-b886-4218-9936-393a7cc40356 36 fields · synced May 30, 2026