ABCFLEX 133000
GUDID 40653405033593
ABCFlex Extension Adapter (Non-sterile)
Conmed Corporation
Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system| Primary Device ID | 40653405033593 |
| NIH Device Record Key | 232a64d8-f3d4-4c30-88fe-1ecdee714d4e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ABCFLEX |
| Version Model Number | 133000 |
| Catalog Number | 133000 |
| 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 | true |
| Serial Number | false |
| 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
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 5 Percent (%) Relative Humidity and 50 Percent (%) Relative Humidity |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 30653405033596 [Primary] |
| GS1 | 40653405033593 [Direct Marking] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K981220
FDA Product Code
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [ABCFLEX]
| 20653405043437 | ABCFLEX FLEXIBLE ENDOSCOPY PROBE [2.3MM (7FR) X 270CM] |
| 20653405043420 | ABCFLEX FLEXIBLE ENDOSCOPY PROBE [2.3MM (7FR) X 220CM] |
| 20653405037887 | ABCFLEX FLEXIBLE ENDOSCOPY PROBE [2.3MM (7FR) X 270CM] |
| 40653405033593 | ABCFlex Extension Adapter (Non-sterile) |
| 20653405032578 | ABCFLEX FLEXIBLE ENDOSCOPY PROBE [2.3MM (7FR) X 220CM] |
Trademark Results [ABCFLEX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ABCFLEX 75936162 2529158 Live/Registered |
ConMed Corporation 2000-03-06 |
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