Primary Device ID | 00859070006050 |
NIH Device Record Key | 03dd2c84-d860-4a42-a3d1-4397018cda56 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LipoGrafter |
Version Model Number | 913000 |
Company DUNS | 187560545 |
Company Name | Musculoskeletal Transplant Foundation, Inc. |
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 | true |
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 | 800-433-6576 |
RA_Licenses@mtf.org |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859070006050 [Primary] |
KYZ | Syringe, Irrigating (Non Dental) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-22 |
Device Publish Date | 2018-09-21 |
W4184420800T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 0.5cc |
W4184420801T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 1CC |
W4184420802T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 2.5CC |
W4184420805T0473 - Legacy DBM | 2022-07-11 Legacy DBM, 5CC |
W4184048010T0479 - DBX® | 2019-06-13 DBX Strip 2.5cm x 10cm |
W4184048015T0479 - DBX® | 2019-06-13 DBX Strip 1.5cm x 1.5cm |
W4184048025T0479 - DBX® | 2019-06-13 DBX Strip 2.5cm x 5cm |
W4184048050T0479 - DBX® | 2019-06-13 DBX Strip 5cm x 5cm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIPOGRAFTER 77934879 3967300 Live/Registered |
Lipocosm, LLC 2010-02-12 |