FDA.reportPublic FDA data

ROTEM®

Primary DI
04260160470587
Brand
ROTEM®
Company
Tem Innovations GmbH
Model
delta System (US/CA)
Catalog number
201001
Device description
The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively.
Published
2018-03-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Product Codes#

Code, Name table
CodeName
GGNPlasma, Coagulation Control
JPASystem, Multipurpose For In Vitro Coagulation Studies

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GGNPlasma, Coagulation ControlHematology2
JPASystem, Multipurpose For In Vitro Coagulation StudiesHematology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K083842000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K083842000ROTEM DELTA THROMBOELASTOMETRY SYSTEMPentapharm GmbH2010-03-23JPA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04260160470587PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04260160470587042601604705874260160470587

GMDN Terms#

Term, Definition table
TermDefinition
Coagulation analyser IVD, laboratory, semi-automatedA mains electricity (AC-powered) laboratory instrument intended to be used for the qualitative and/or quantitative in vitro determination of one or multiple coagulation components involved in haemostasis in a clinical specimen [e.g., performs tests such as prothrombin time (PT), partial thromboplastin time (PTT)]. Analyser design may incorporate spectrophotometry, turbidimetry, nephelometry, electrometry and/or mechanical means of clot formation or end point detection. The device operates with reduced technician involvement and automation of some, but not all, procedural steps.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
506692297
Device count
1
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04260160470327ROTEM®sigma complete + hep5555022022-10-04
04260160470341ROTEM®sigma ROTROL N5552012022-10-04
04260160470358ROTEM®sigma ROTROL P5552022022-10-04
04260160470044ROTEM®in-tem®503-02-US2016-09-16
04260160470068ROTEM®ap-tem®503-04-US2016-09-16
04260160470075ROTEM®fib-tem®503-06-US2016-09-16
04260160470082ROTEM®hep-tem®503-09-US2016-09-16
04260160470099ROTEM®star-tem® 20503-10-US2016-09-16
04260160470105ROTEM®ROTROL N503-24-US, 503-242016-09-16
04260160470112ROTEM®ROTROL P503-25-US, 503-252016-09-16
04260160470242ROTEM®ex-tem®503-05-US2016-09-16
04260160470600ROTEM®sigma complete + hep5555022022-10-04
04260160470617ROTEM®sigma ROTROL N5552012022-10-04
04260160470624ROTEM®sigma ROTROL P5552022022-10-04
04260160470372ROTEM®sigma2110002022-10-04
04260160470020ROTEM®delta System200100-US2016-09-16

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Primary DI, Brand, Company table
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20763000558189CLOTtrac™MEDTRONIC, INC.JPA2026-02-22
20763000558295RACTMEDTRONIC, INC.JPA2026-02-22
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