Centurion
GUDID 10653160217381
CENTURION MEDICAL PRODUCTS CORPORATION
Pelvic examination kit| Primary Device ID | 10653160217381 |
| NIH Device Record Key | e0f49146-e501-4bf8-a347-f85142849578 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Centurion |
| Version Model Number | PE2870 |
| Company DUNS | 017246562 |
| Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 00653160217384 [Primary] |
| GS1 | 10653160217381 [Package] Contains: 00653160217384 Package: CASE [14 Units] In Commercial Distribution |
FDA Product Code
| MLT | Pelvic exam 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 | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-11-11 |
On-Brand Devices [Centurion]
Trademark Results [Centurion]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.