CathGrip
GUDID 10653599002190
CathGrip Single Strap, Small, Non-Sterile, No Wipes, Brazil
ARGENTUM MEDICAL, LLC
Wearable percutaneous catheter/tube holder| Primary Device ID | 10653599002190 |
| NIH Device Record Key | 1518e6cf-3167-4e96-98c2-d4eaf805a509 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CathGrip |
| Version Model Number | 51250NSNWBR |
| Company DUNS | 091449079 |
| Company Name | ARGENTUM MEDICAL, LLC |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com | |
| Phone | 800-864-6755 |
| CustomerCare@BioDermInc.com |
Operating and Storage Conditions
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 10 Degrees Celsius and 30 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653599002193 [Primary] |
| GS1 | 10653599002190 [Package] Contains: 00653599002193 Package: box [30 Units] In Commercial Distribution |
FDA Product Code
| KMK | Device, Intravascular Catheter Securement |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-10 |
| Device Publish Date | 2024-05-31 |
On-Brand Devices [CathGrip]
| 10653599001865 | CathGrip Oval, Medium, Sterile, No Alcohol |
| 10653599001063 | CathGrip Oval, Medium, Non-Sterile for Medline Nutritional |
| 10653599000936 | CathGrip Oval, Small, Non-Sterile for Medline Nutritional |
| 10653599000929 | CathGrip Single Strap, Large, Non-Sterile for Medline Nutritional |
| 10653599000547 | CathGrip Single Strap Large, Non-Sterile, No Alcohol |
| 10653599002244 | CathGrip Oval, Large, Non-Sterile, No Wipes, Brazil |
| 10653599002237 | CathGrip Oval, Small, Non-Sterile, No Wipes, Brazil |
| 10653599002220 | CathGrip Single Strap, Large, Non-Sterile, No Wipes, Brazil |
| 10653599002213 | CathGrip Double Strap, Medium, Non-Sterile, No Wipes, Brazil |
| 10653599002206 | CathGrip Double Strap, Large, Non-Sterile, No Wipes, Brazil |
| 10653599002190 | CathGrip Single Strap, Small, Non-Sterile, No Wipes, Brazil |
Trademark Results [CathGrip]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CATHGRIP 87077049 5128749 Live/Registered |
BioDerm, Inc. 2016-06-20 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.