Primary Device ID | 17350025911035 |
NIH Device Record Key | 8135fd5c-7cfc-4534-b27d-0b5f0e85cfd3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Follicle Aspiration Set, Single Lumen |
Version Model Number | 14104 |
Company DUNS | 631805488 |
Company Name | Vitrolife Sweden AB |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07350025911038 [Primary] |
GS1 | 17350025911035 [Package] Contains: 07350025911038 Package: [10 Units] In Commercial Distribution |
MQE | Needle, Assisted Reproduction |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-09 |
17350025914852 | 14183 |
17350025914241 | 14169 |
17350025911561 | 14157 |
17350025911554 | 14156 |
17350025911448 | 14145 |
17350025911387 | 14186 |
17350025911370 | 14185 |
17350025911349 | 14135 |
17350025911318 | 14132 |
17350025911295 | 14130 |
17350025911257 | 14126 |
17350025911240 | 14125 |
17350025911196 | 14120 |
17350025911189 | 14119 |
17350025911158 | 14116 |
17350025911127 | 14113 |
17350025911110 | 14112 |
17350025911066 | 14107 |
17350025911035 | 14104 |
07350025911021 | 14103 |
17350025911004 | 14101 |