LIGHTWAVE IA-2000-S
GUDID 20845854040345
LIGHTWAVE SUCTION ABLATOR
Conmed Corporation
Open-surgery electrosurgical electrode, monopolar, single-use| Primary Device ID | 20845854040345 |
| NIH Device Record Key | c83d6929-ee3e-486b-93d8-cfb864cc9920 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LIGHTWAVE |
| Version Model Number | IA-2000-S |
| Catalog Number | IA-2000-S |
| 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 | 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854040345 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K083281
FDA Product Code
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [LIGHTWAVE]
| 20845854040369 | LIGHTWAVE ABLATOR 90 DEGREE ANGLE 3.2MM X 150MM |
| 20845854040352 | LIGHTWAVE ABLATOR, 90 DEGREE ANGLE, 3.2MM X 150MM |
| 20845854040345 | LIGHTWAVE SUCTION ABLATOR |
| 10845854040348 | LightWave Suction Ablator |
Trademark Results [LIGHTWAVE]
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