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AutoDELFIA Neonatal IRT kit

FDA UDI

Class I (US FDA UDI)

by Wallac, Inc.

Identity

Trade Name
AutoDELFIA Neonatal IRT kit FDA UDI
Generic Name
Neonatal trypsin IVD, kit, fluorescent immunoassay FDA UDI
Device Name
For the quantitative determination of immunoreactive trypsin (IRT) in dried blood. FDA UDI
Model / Reference
B005-204 FDA UDI
Description
For the quantitative determination of immunoreactive trypsin (IRT) in dried blood. FDA UDI

Identifiers

Catalog Number
B005-204 FDA UDI
Primary DI / UDI-DI
06438147298785 FDA UDI
510(k) Number
K110274 FDA UDI
FDA Product Code
JNO FDA UDI
GMDN Term
Neonatal trypsin IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1725 FDA UDI
Commercial Distribution
Not 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

No

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

AutoDELFIA Neonatal IRT kit by Wallac, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K110274 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wallac, Inc.

Sources (1)

  • FDA UDI 74faf6be-cecf-4296-b029-e01566be37fa 37 fields · synced May 30, 2026