AccessGUDID - DEVICE: FLEX Mono Mo A-Hu CD30 Cl Ber-H2 RTU (Link) (05700572029144)

GUDID

Device Identifier (DI) Information

Brand Name: FLEX Mono Mo A-Hu CD30 Cl Ber-H2 RTU (Link)
Version or Model: IR602
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: AGILENT TECHNOLOGIES SINGAPORE PTE LTD

Primary DI Number: 05700572029144
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 894671143 *Terms of Use

Device Description: FLEX Monoclonal Mouse Anti-Human CD30 Clone Ber-H2 Ready-to-Use (Link)

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?
56968	Tumour necrosis factor receptor superfamily IVD, antibody	One or multiple immunoglobulins capable of binding to specific antigenic determinants and intended to be used for the qualitative and/or quantitative detection of one or multiple members of the tumour necrosis factor receptor superfamily (e.g., GITR, TNFR1, 4-1BB) in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NJT	IMMUNOHISTOCHEMISTRY REAGENTS AND KITS

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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
Device Size Text, specify: 40-60 Tests

Device Record Status

Public Device Record Key: 74d7f6ee-bc6d-4fe0-a043-53b88ad419d3
Public Version Date: January 20, 2023
Public Version Number: 3
DI Record Publish Date: September 17, 2020