Primary Device ID | 20811998034137 |
NIH Device Record Key | 9b7bdc24-1714-4e69-bb57-4b4841edcf9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OIC Variable Angle Small Fragment Locking Plate Sy |
Version Model Number | KW200-150 |
Company DUNS | 070061160 |
Company Name | ORTHOPAEDIC IMPLANT COMPANY, THE |
Device Count | 10 |
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 | true |
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 | 775 636 8281 |
Info@OrthoImplantCompany.com | |
Phone | 775 636 8281 |
Info@OrthoImplantCompany.com |
Length | 150 Millimeter |
Outer Diameter | 2 Millimeter |
Length | 150 Millimeter |
Outer Diameter | 2 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10811998034130 [Unit of Use] |
GS1 | 20811998034137 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[20811998034137]
Moist Heat or Steam Sterilization
[20811998034137]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-08-31 |
Device Publish Date | 2018-07-31 |
20811998034137 | K-WIRE (10/PACK) 2.0MM X 150MM |
20811998034120 | K-WIRE (10/PACK) 1.6MM X 150MM |
20811998034113 | K-WIRE (10/PACK) 1.25MM X 150MM |