Primary Device ID | 10841307123668 |
NIH Device Record Key | d46b0d5b-842e-4061-b058-b393733e5d29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical Kit Grommet - Small (2pk) |
Version Model Number | SKG- S |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
Device Count | 2 |
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 | false |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841307123661 [Unit of Use] |
GS1 | 10841307123668 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
[10841307123668]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-10-21 |
Device Publish Date | 2017-06-23 |