AccessGUDID - DEVICE: INTRA UTERINE INSEMINATION CANNULA WITH MANDREL (03700111400566)

GUDID

Device Identifier (DI) Information

Brand Name: INTRA UTERINE INSEMINATION CANNULA WITH MANDREL
Version or Model: INTRA UTERINE INSEMINATION CANNULA WITH MANDREL
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 12040AM
Company Name: LABORATOIRE CCD

Primary DI Number: 03700111400566
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 381633924 *Terms of Use

Device Description: Catheter /probe for artificial insemination

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?
45846	Assisted reproduction transfer catheter/set	A device or collection of devices that includes a flexible polymer tube intended to be used primarily to transfer gametes (eggs or sperm) and/or embryos into the female reproductive tract for the purpose of assisted reproduction [e.g., intrauterine insemination (IUI) or gamete intrafallopian transfer (GIFT)]. In addition to the ‘live transfer’ catheter it may also include a trial transfer catheter intended to assess/ensure that embryo placement will be successful; it typically also includes devices intended to assist catheter introduction (e.g., outer guide sheath, stylet). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HDR	CAP, CERVICAL

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: -The product must not be used in the event of damaged, or open primary packaging before the medical procedure. -Store away from direct sunlight. -Store in a dry place.

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 0.21 Centimeter
Catheter Length: 17.5 Centimeter

Device Record Status

Public Device Record Key: 88766599-42ff-43ec-9185-0bb9b5de7159
Public Version Date: December 13, 2023
Public Version Number: 1
DI Record Publish Date: December 05, 2023