Primary Device ID | 17350025915583 |
NIH Device Record Key | 8f2f9dc8-34a6-4df4-9dda-9d3c8f7e0c59 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cyst Puncture Needle with Stylet |
Version Model Number | 17806 |
Company DUNS | 631805488 |
Company Name | Vitrolife Sweden AB |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 07350025915586 [Primary] |
GS1 | 17350025915583 [Package] Contains: 07350025915586 Package: [10 Units] In Commercial Distribution |
KNA | Instrument, Manual, Specialized Obstetric-Gynecologic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-01-09 |
17350025915637 | 17812 |
17350025915620 | 17811 |
17350025915606 | 17809 |
17350025915583 | 17806 |
17350025915576 | 17805 |
17350025915552 | 17803 |
17350025912391 | 14812 |
17350025912384 | 14811 |
17350025912360 | 14809 |
07350025912332 | 14806 |
07350025912325 | 14805 |
07350025912301 | 14803 |