CATHETER
GUDID 00888118057709
KLS-Martin L.P.
Eustachian catheter, reusable| Primary Device ID | 00888118057709 |
| NIH Device Record Key | 5dd095c1-1c55-4428-85a2-663994c3712b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CATHETER |
| Version Model Number | 36-321-03-01 |
| 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 |
Customer Support Contacts
| 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 Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888118057709 [Primary] |
FDA Product Code
| GBY | CATHETER, EUSTACHIAN, GENERAL & PLASTIC SURGERY |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
[00888118057709]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-02-20 |
| Device Publish Date | 2018-09-26 |
On-Brand Devices [CATHETER]
| 00888118057709 | 36-321-03-01 |
| 00888118057693 | 36-321-02-01 |
| 00888118057686 | 36-321-01-01 |
Trademark Results [CATHETER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CATHETER 75933670 2499805 Dead/Cancelled |
Ecuyer, Robert Anthony 2000-03-02 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.