Primary Device ID | 08806390895002 |
NIH Device Record Key | 102e663a-b7f5-4572-8c95-1c0bd7029d19 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prometheus System Surgical Instrument |
Version Model Number | PRO-90090 |
Company DUNS | 688811603 |
Company Name | Jeil Medical Corporation |
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 | 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 | 08806390895002 [Primary] |
HXW | Bender |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
Moist Heat or Steam Sterilization
[08806390895002]
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 |