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Pancreatic Elastase ELISA

FDA UDI

Class I (US FDA UDI)

by Seramun Diagnostica GmbH

Identity

Trade Name
Pancreatic Elastase ELISA FDA UDI
Generic Name
Pancreatic elastase (PE) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
G09040 FDA UDI

Identifiers

Primary DI / UDI-DI
04099466112248 FDA UDI
FDA Product Code
JNO FDA UDI
GMDN Term
Pancreatic elastase (PE) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1725 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pancreatic elastase (PE) IVD, kit, enzyme immunoassay (EIA)

Pancreatic Elastase ELISA by Seramun Diagnostica GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pancreatic elastase (PE) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c25ee029-7ba7-447c-93ef-997a29f8ae87 32 fields · synced May 31, 2026