Primary Device ID | 03700569645878 |
NIH Device Record Key | 6aff4300-64e1-4496-aa0b-95c5fdc24aba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Activmotion S |
Version Model Number | BTDMD2D-ST |
Catalog Number | BTDMD2D-ST |
Company DUNS | 263281904 |
Company Name | NEWCLIP TECHNICS |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700569645878 [Primary] |
HRS | Plate, Fixation, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-21 |
Device Publish Date | 2024-11-13 |
03700569671105 | BATDMD2D-ST |
03700569671099 | BATGMD2D-ST |
03700569671082 | BATDMD1D-ST |
03700569671075 | BATGMD1D-ST |
03700569645953 | BTGMD2D-ST |
03700569645946 | BTGMD2D |
03700569645939 | BTGMD1D-ST |
03700569645922 | BTGBD2D-ST |
03700569645915 | BTGBD2D |
03700569645908 | BTGBD1D-ST |
03700569645885 | BTGMD1D |
03700569645878 | BTDMD2D-ST |
03700569645861 | BTDMD2D |
03700569645854 | BTDMD1D-ST |
03700569645847 | BTDMD1D |
03700569645830 | BTDBD2D-ST |
03700569645823 | BTDBD2D |
03700569645816 | BTDBD1D-ST |
03700569645809 | BTDBD1D |
03700569642266 | ATGP2D-ST |
03700569642259 | ATGP2D |
03700569642242 | ATGP1D-ST |
03700569642235 | ATGP1D |
03700569642228 | ATDP2D-ST |
03700569642211 | ATDP2D |
03700569642204 | ATDP1D-ST |