Primary Device ID | 25425017502016 |
NIH Device Record Key | efd1e2fe-b28d-47e8-830c-1feb44b23420 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Intrauterine insemination cannula |
Version Model Number | #4220 IUI Memo |
Company DUNS | 283088573 |
Company Name | Gynetics Medical Products NV |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +3211645872 |
info@gynetics.com |
Length | 206 Millimeter |
Storage Environment Temperature | Between 0 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05425017502012 [Primary] |
GS1 | 15425017502019 [Package] Contains: 05425017502012 Package: [25 Units] In Commercial Distribution |
GS1 | 25425017502016 [Package] Contains: 05425017502012 Package: [125 Units] In Commercial Distribution |
MQF | Catheter, Assisted Reproduction |
Steralize Prior To Use | true |
Device Is Sterile | true |
[25425017502016]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-01-23 |
Device Publish Date | 2016-11-03 |
15425017502088 | Intrauterine insemination cannula |
25425017502061 | Intrauterine insemination cannula |
25425017502054 | Intrauterine insemination cannula |
25425017502047 | Intrauterine insemination cannula |
25425017502030 | Intrauterine insemination cannula |
25425017502023 | Intrauterine insemination cannula |
25425017502016 | Intra uterine Artificial Insemination |
25425017502009 | Intra uterine Artificial Insemination |