Primary Device ID | 17350025915101 |
NIH Device Record Key | 0dfcb907-2ceb-459c-9ab6-01ddfe11008c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Follicle Aspiration Set Single Lumen |
Version Model Number | 17107 |
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 | 07350025915104 [Primary] |
GS1 | 17350025915101 [Package] Contains: 07350025915104 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 | 2017-09-22 |
17350025915514 | 17186 |
17350025915507 | 17185 |
17350025915491 | 17183 |
17350025915385 | 17157 |
17350025915378 | 17156 |
17350025915309 | 17145 |
17350025915262 | 17132 |
17350025915248 | 17130 |
17350025915224 | 17126 |
17350025915217 | 17125 |
17350025915194 | 17120 |
17350025915187 | 17119 |
17350025915170 | 17116 |
17350025915156 | 17113 |
17350025915149 | 17112 |
17350025915101 | 17107 |
17350025915088 | 17104 |
17350025915071 | 17103 |
17350025915699 | 17189 |