Centurion
GUDID 10653160239505
CENTURION MEDICAL PRODUCTS CORPORATION
Peripheral intravenous catheterization support kit| Primary Device ID | 10653160239505 |
| NIH Device Record Key | b71c1287-15e8-4680-916f-11a43b31955b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Centurion |
| Version Model Number | CVI3385 |
| Company DUNS | 017246562 |
| Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
| 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 | true |
| Device Combination Product | true |
| 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)248-4058 |
| CUSTOMERSERVICE@CENTURIONMP.COM | |
| Phone | +1(800)248-4058 |
| CUSTOMERSERVICE@CENTURIONMP.COM |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653160239508 [Primary] |
| GS1 | 10653160239505 [Package] Contains: 00653160239508 Package: CASE [15 Units] In Commercial Distribution |
FDA Product Code
| LRS | I.V. start kit |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2017-08-14 |
On-Brand Devices [Centurion]
Trademark Results [Centurion]
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