Primary Device ID | 00888118030337 |
NIH Device Record Key | d8527f07-abff-4020-84a5-884544eb04fa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RONGEUR |
Version Model Number | 23-807-16-07 |
Company DUNS | 826499238 |
Company Name | KLS-Martin L.P. |
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 | 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 |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com | |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com |
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 | 00888118030337 [Primary] |
HTX | RONGEUR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
[00888118030337]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2018-09-26 |