FDA UDI In Commercial Distribution 🇺🇸 United States

ROTEM®

DI: 04260160470372 · Model: sigma · Tem Innovations GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROTEM®
Primary DI
04260160470372
Version / Model
sigma
Catalog Number
211000
Company Name
Tem Innovations GmbH
Labeler DUNS
506692297
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-04
Public Version
1
Public Version Date
2022-10-12
Public Version Status
New
Public Device Record Key
14bf03af-8f48-44a6-b28a-3ea43b897da5

Device Description

The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses. Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JPA System, Multipurpose For In Vitro Coagulation Studies

GMDN Terms

Code Name
56689 Coagulation analyser IVD, laboratory

Identifiers

Type ID
Primary 04260160470372

Premarket Submissions

Submission Number Supplement Number
K201440 000