Flexvision 0233032800
GUDID 07613327051490
Sterilization Tray for Flexible Urology Instruments
STRYKER CORPORATION
Sterilization container| Primary Device ID | 07613327051490 |
| NIH Device Record Key | 31c4bbed-4cc6-4369-ae32-11ecfa603b64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Flexvision |
| Version Model Number | 0233032800 |
| Catalog Number | 0233032800 |
| Company DUNS | 187502109 |
| Company Name | STRYKER 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327051490 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K935237
FDA Product Code
| FGB | Ureteroscope and accessories, flexible/rigid |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
[07613327051490]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
Devices Manufactured by STRYKER CORPORATION
| 07613327661989 - KNOTILUS+ | 2025-06-24 2.9X15.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
| 07613327661996 - KNOTILUS+ | 2025-06-24 2.4X8.9MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE |
| 07613327662009 - KNOTILUS+ | 2025-06-24 2.4X11.3MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
| 07613327662016 - KNOTILUS+ | 2025-06-24 2.9X12.5MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE |
| 07613327662023 - KNOTILUS+ | 2025-06-24 2.9X12.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE |
| 07613327662030 - ALPHAVENT | 2025-06-24 ALPHAVENT KNOTLESS SP, 4.75MM, BIOCOMPOSITE ANCHOR |
| 07613327662047 - ALPHAVENT | 2025-06-24 ALPHAVENT KNOTLESS SP, 5.5MM, BIOCOMPOSITE ANCHOR |
| 07613327662054 - ALPHAVENT | 2025-06-24 ALPHAVENT KNOTLESS SP, 6.5MM, BIOCOMPOSITE ANCHOR |
Trademark Results [Flexvision]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FLEXVISION 76573259 3036319 Dead/Cancelled |
Stryker Corporation 2004-01-30 |
 FLEXVISION 75649768 2321530 Dead/Cancelled |
Flexstrip Products International, Inc. 1999-03-01 |
 FLEXVISION 74608043 1997897 Live/Registered |
ASA ELECTRONICS, LLC 1994-12-07 |
 FLEXVISION 73514844 1386566 Dead/Cancelled |
OBJECT RECOGNITION SYSTEMS, INC. 1984-12-20 |
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