CRYSTALVIEW CV4000
GUDID 10845854648506
CrystalView™ Pro Irrigation Console
Conmed Corporation
Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system Arthroscopic irrigation/insufflation system| Primary Device ID | 10845854648506 |
| NIH Device Record Key | 6d5f958c-127d-4e2f-85f1-b6d533ddc22c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CRYSTALVIEW |
| Version Model Number | CV4000 |
| Catalog Number | CV4000 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854648506 [Direct Marking] |
| GS1 | 10845854850381 [Previous] |
| GS1 | 30845854648500 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K182882
FDA Product Code
| HRX | Arthroscope |
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 | 2020-09-01 |
| Device Publish Date | 2020-08-24 |
On-Brand Devices [CRYSTALVIEW]
| 10845854850381 | CrystalView™ Pro Irrigation Console |
| 10845854648506 | CrystalView™ Pro Irrigation Console |
| 10653405987505 | CrystalView™ Pro Irrigation Console |
| 30845854648517 | CrystalView™ Pro Autoclavable Remote Control |
Trademark Results [CRYSTALVIEW]
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.