Centurion
GUDID 10653160281542
CENTURION MEDICAL PRODUCTS CORPORATION
Contact lens case| Primary Device ID | 10653160281542 |
| NIH Device Record Key | e791be92-cdec-4f22-8197-6333516facfb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Centurion |
| Version Model Number | LENSHOLDB20 |
| Company DUNS | 017246562 |
| Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
| Device Count | 20 |
| 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 | 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 | 00010164490203 [Unit of Use] |
| GS1 | 00653160281545 [Primary] |
| GS1 | 10653160281542 [Package] Contains: 00653160281545 Package: EACH [20 Units] In Commercial Distribution |
FDA Product Code
| LRX | Case, contact lens |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-08-23 |
On-Brand Devices [Centurion]
Trademark Results [Centurion]
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