Centurion LC305
GUDID 00653160322156
STERILE LINE CHANGE KIT
CENTURION MEDICAL PRODUCTS CORPORATION
General surgical procedure kit, medicated| Primary Device ID | 00653160322156 |
| NIH Device Record Key | b80cb0db-4544-4608-8443-7f891749d12b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Centurion |
| Version Model Number | LC305 |
| Catalog Number | LC305 |
| 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653160322156 [Package] Contains: 10653160322153 Package: CASE [20 Units] In Commercial Distribution |
| GS1 | 10653160322153 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K213481
FDA Product Code
| LRO | General Surgery Tray |
| LRP | TRAY, SURGICAL |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-01-10 |
| Device Publish Date | 2022-01-01 |
On-Brand Devices [Centurion]
Trademark Results [Centurion]
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.