Primary Device ID | 08806390897747 |
NIH Device Record Key | b3ce1dc4-401b-445f-a522-fb22f5d14140 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prometheus System Bone Screw |
Version Model Number | PRO-10228 |
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 | 08806390897747 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
[08806390897747]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |