Centurion
GUDID 10653160197485
CENTURION MEDICAL PRODUCTS CORPORATION
Surgical penis clamp, single-use| Primary Device ID | 10653160197485 |
| NIH Device Record Key | 1f0deb58-f5a6-4e55-8204-f978bb4efbb4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Centurion |
| Version Model Number | 3145CR |
| Company DUNS | 017246562 |
| Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 | 00653160197488 [Primary] |
| GS1 | 10653160197485 [Package] Contains: 00653160197488 Package: CASE [12 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K890897
FDA Product Code
| HFX | CLAMP, CIRCUMCISION |
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 | 2020-05-04 |
| Device Publish Date | 2016-08-31 |
On-Brand Devices [Centurion]
Trademark Results [Centurion]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.