Primary Device ID | 00810041639783 |
NIH Device Record Key | 430821e7-441b-4763-abb1-263988bb61ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Smith and Nephew |
Version Model Number | 25-1810 |
Company DUNS | 016889401 |
Company Name | Provision |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com | |
Phone | 541-480-7953 |
customersupport@provisiondrs.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810041639783 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-09 |
Device Publish Date | 2020-10-30 |