Primary Device ID | 08809488211791 |
NIH Device Record Key | 6f426372-03d5-41be-a66a-d0d5fb7ade0a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KJ SUBMERGED SYSTEM - SH Abutment |
Version Model Number | PTAB2062S |
Company DUNS | 688476027 |
Company Name | KJMEDITECH.CO.,LTD |
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 | 08809488211791 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08809488211791]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-08-26 |
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08809488211982 | PTAB35056S |
08809488211975 | PTAB36054S |
08809488211968 | PTAB35054S |
08809488211951 | PTAB55066S |
08809488211944 | PTAB54066S |
08809488211937 | PTAB55064S |
08809488211920 | PTAB54064S |
08809488211913 | PTAB24576S |
08809488211906 | PTAB23566S |
08809488211890 | PTAB24574S |
08809488211883 | PTAB23564S |
08809488211876 | PTAB3062S |
08809488211869 | PTAB3061S |
08809488211852 | PTAB3042S |
08809488211845 | PTAB3041S |
08809488211838 | PTAB2362S |
08809488211821 | PTAB2361S |
08809488211814 | PTAB2342S |
08809488211807 | PTAB2341S |
08809488211791 | PTAB2062S |
08809488211784 | PTAB2061S |
08809488211777 | PTAB2042S |
08809488211760 | PTAB2041S |