AccessGUDID - DEVICE: DBC Total Estrogens ELISA (B261CANE6308PK0)

GUDID

Device Identifier (DI) Information

Brand Name: DBC Total Estrogens ELISA
Version or Model: CAN-E-630-8PK
Commercial Distribution Status: In Commercial Distribution
Catalog Number: CAN-E-630-8PK
Company Name: Diagnostics Biochem Canada Inc

Primary DI Number: B261CANE6308PK0
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 207718438 *Terms of Use

Device Description: For the quantitative measurement of Total Estrogens in human serum by an ELISA (Enzyme-Linked Immunosorbent Assay). For in vitro diagnostic use.

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):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
63754	Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA)	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of total estrogen (oestrogen) hormones [estradiol, estriol, and estrone] in a clinical specimen, using an enzyme immunoassay (EIA) method. It is used as an aid in the diagnosis of sex steroid metabolism-related conditions (e.g., premature or delayed puberty), or assessment of fracture risk and monitoring of hormone replacement therapy in postmenopausal women.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JMD	Radioimmunoassay, Total Estrogens, Nonpregnancy

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
No Device Sizes

Device Record Status

Public Device Record Key: 120db5f8-18a8-4887-b1f4-cf3214a209c8
Public Version Date: November 18, 2022
Public Version Number: 1
DI Record Publish Date: November 10, 2022