Primary Device ID | 08800089411832 |
NIH Device Record Key | a21b7cf2-0f10-4c77-a2d9-635f6bf145dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INLET System Bone Screw |
Version Model Number | IN20L-HF-014 |
Company DUNS | 688811603 |
Company Name | Jeil Medical Corporation |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800089411832 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
[08800089411832]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-23 |
Device Publish Date | 2021-11-15 |