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ScheBo® Pancreatic Elastase 1™

FDA UDI

Class I (US FDA UDI)

by ScheBo r. Biotech Aktiengesellschaft

Identity

Trade Name
ScheBo® Pancreatic Elastase 1™ FDA UDI
Generic Name
Pancreatic elastase (PE) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
ELISA Stool Test FDA UDI

Identifiers

Catalog Number
07 FDA UDI
Primary DI / UDI-DI
04260152080701 FDA UDI
FDA Product Code
JNN 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

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

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)

ScheBo® Pancreatic Elastase 1™ by ScheBo r. Biotech Aktiengesellschaft — 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 82b5359b-2d66-49f7-b254-48c6bcabb7c6 33 fields · synced May 30, 2026