Primary Device ID | 10705034005232 |
NIH Device Record Key | 58228a89-c6a5-40ec-bee6-44b9898f3288 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KANEDA SR |
Version Model Number | 3210510 |
Catalog Number | 3210510 |
Company DUNS | 482661753 |
Company Name | Medos International Sàrl |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705034005232 [Primary] |
HWJ | AWL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2016-12-31 |
10705034005270 | KANEDA SR ANTERIOR SYSTEM PLATE HOLDER |
10705034005232 | KANEDA SR ANTERIOR SYSTEM ANGLED AWL (MODULAR) |
10705034005225 | KANEDA SR ANTERIOR SYSTEM AWL (MODULAR) |