Primary Device ID | 03700569642372 |
NIH Device Record Key | b372b615-fb50-4972-8dbe-ef17348e769a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Xpert Wrist |
Version Model Number | BDT1.8L20-ST |
Catalog Number | BDT1.8L20-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 | 03700569642372 [Primary] |
HWC | Screw, 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 |
03700569654382 | CAT3.5L18D-ST |
03700569654375 | CAT3.5L18D |
03700569654368 | CAT3.5L16D-ST |
03700569654351 | CAT3.5L16D |
03700569654344 | CAT3.5L14D-ST |
03700569654337 | CAT3.5L14D |
03700569654320 | CAT3.5L12D-ST |
03700569654313 | CAT3.5L12D |
03700569654306 | CAT3.5L10D-ST |
03700569654290 | CAT3.5L10D |
03700569642402 | BDT1.8L26-ST |
03700569642396 | BDT1.8L24-ST |
03700569642389 | BDT1.8L22-ST |
03700569642372 | BDT1.8L20-ST |
03700569642365 | BDT1.8L18-ST |
03700569642358 | BDT1.8L16-ST |
03700569642341 | BDT1.8L14-ST |
03700569642334 | BDT1.8L26 |
03700569642327 | BDT1.8L24 |
03700569642310 | BDT1.8L22 |
03700569642303 | BDT1.8L20 |
03700569642297 | BDT1.8L18 |
03700569642280 | BDT1.8L16 |
03700569642273 | BDT1.8L14 |