First PICC™ D/L Peripherally Inserted Central Catheter 384159
GUDID 20886333209709
First PICC™ D/L Peripherally Inserted Central Catheter 16ga (5F) 1.75mm x 65cm
ARGON MEDICAL DEVICES, INC.
Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter| Primary Device ID | 20886333209709 |
| NIH Device Record Key | f2b10db4-5159-4dfb-8bae-dcf2131ab9c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | First PICC™ D/L Peripherally Inserted Central Catheter |
| Version Model Number | 384159 |
| Catalog Number | 384159 |
| Company DUNS | 140727624 |
| Company Name | ARGON MEDICAL DEVICES, INC. |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
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 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 |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333209705 [Primary] |
| GS1 | 20886333209709 [Package] Contains: 00886333209705 Package: Box [5 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K972263
FDA Product Code
| FOZ | Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-21 |
Devices Manufactured by ARGON MEDICAL DEVICES, INC.
| 20886333227598 - Intara™ Introducer Sheath | 2024-06-21 Intara™ Introducer Sheath 10F x 41.5cm |
| 00886333227167 - CLEANER Vac™ | 2024-04-25 CLEANER Vac™ Thrombectomy System - 18F OD x 115cm |
| 00886333227174 - Cleaner Vac™ | 2024-04-25 Cleaner Vac™ - 18F OD x 115cm Aspiration Catheter with Handpiece |
| 00886333227624 - Cleaner Vac™ | 2024-04-25 Cleaner Vac™ Aspiration Canister |
| 00886333225743 - Kodiak | 2023-07-10 Kodiak™ Dual Port Coaxial Introducer Kit |
| 20886333227284 - Co-Axial Introducer Needle | 2023-06-16 Co-Axial Introducer Needle 15ga x 6.8cm |
| 20886333227383 - Percutaneous Introducer | 2023-04-19 Percutaneous Introducer with Depth Marks 4F x 25cm |
| 20886333227390 - Percutaneous Introducer | 2023-04-19 Percutaneous Introducer with Depth Marks 4F x 45cm |
Trademark Results [First PICC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FIRST PICC 74637602 2084417 Live/Registered |
ARGON MEDICAL DEVICES, INC. 1995-02-23 |
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