Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9614972

FEI Number

3003780132

Entity Name

SCHEBO BIOTECH AG

City/State/Country

GIESSEN Hesse, DE

Establishment Address

NETANYASTRASSE 3-5, GIESSEN Hesse 35394, DE

Establishment Type(s)

Manufacture Medical Device,Foreign Private Label Distributor

Owner / Operator

SCHEBO BIOTECH AG (Owner Number: 9032007)

Owner / Operator Contact Address

NETANYASTRASSE 3, --, GIESSEN, DE-NOTA 35394, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pancreatic Elastase 1 Stool Test ScheBo Master Quick-Prep

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JNN	P-Toluenesulphonyl-L-Arginine Methyl Ester (U.V.), Trypsin	Clinical Chemistry	Class 1	862.1725	2008-02-07
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2017-08-17

Official Correspondent

Rene Kroeger

US Agent Details

Sonja Kammerer Business: SCHEBO BIOTECH USA, INC. Email: info@schebousa.com Phone: (254) 3716978

Related Public Records

Same Entity

SCHEBO BIOTECH AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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3004061467	R-BIOPHARM AG	DARMSTADT Hesse, DE
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9614972. Last updated year: 2026. Please use registration number 9614972 when referencing this establishment in official correspondence.