AccessGUDID - DEVICE: Thermo Scientific Pacific Hemostasis® (00845275000825)

GUDID

Device Identifier (DI) Information

Brand Name: Thermo Scientific Pacific Hemostasis®
Version or Model: 100600
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Fisher Diagnostics

Primary DI Number: 00845275000825
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 9
Labeler D-U-N-S® Number*: 183998769 *Terms of Use

Device Description: No description.

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:	Yes
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?
55997	Fibrinogen assay (factor I) IVD, kit, clotting	A collection of reagents and other associated materials intended to be used for the quantitative measurement of fibrinogen (factor I) in a clinical specimen, using a clotting method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GIS	Test, Fibrinogen

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K023362	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: ec6bcd21-fa1b-42bf-acaf-f11b3191891d
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: September 16, 2016