AccessGUDID - DEVICE: Dade Actin Activated Cephaloplastin Reagent (00630414640310)

GUDID

Device Identifier (DI) Information

Brand Name: Dade Actin Activated Cephaloplastin Reagent
Version or Model: 10873827
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 10873827
Company Name: Siemens Healthcare Diagnostics Products GmbH

Primary DI Number: 00630414640310
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 10
Labeler D-U-N-S® Number*: 388240673 *Terms of Use

Device Description: Liquid rabbit brain cephalin with plasma activator for coagulation procedures requiring the determination of activated partial thromboplastin time

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
55982	Activated partial thromboplastin time (APTT) IVD, reagent	A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the quantitative measurement of the activated partial thromboplastin time (APTT) of a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GFO	ACTIVATED PARTIAL THROMBOPLASTIN

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K760318	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b9b7ba63-d280-4d8a-9cbe-0753910dffbf
Public Version Date: April 02, 2024
Public Version Number: 1
DI Record Publish Date: March 25, 2024