Primary Device ID | 08800089431069 |
NIH Device Record Key | 07eb3076-75b2-48e8-b9d0-0601ad40fd56 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical Instrument |
Version Model Number | 111-380 |
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 | 08800089431069 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
[08800089431069]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-14 |
Device Publish Date | 2025-05-06 |