Primary Device ID | 00860003755525 |
NIH Device Record Key | d3faf405-065c-4078-af58-741bd68add65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FastForward |
Version Model Number | 1700-00-002 |
Company DUNS | 117495281 |
Company Name | FASTFORWARD SURGICAL INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | 00860003755525 [Primary] |
HTN | Washer, Bolt Nut |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-20 |
Device Publish Date | 2020-07-12 |
00860003755525 | Plate, FastForward, Small |
00860003755518 | Plate, FastForward, Medium |
00860003755532 | Plate, FastFoward, Large |