Sensimatic™ D703-K
GUDID 00810000520107
Indifferent Plate and Cable for Sensimatic® 700SE (Korea)
PARKELL, INC.
Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable| Primary Device ID | 00810000520107 |
| NIH Device Record Key | 95530f90-16ca-4998-bd99-23a35605755d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sensimatic™ |
| Version Model Number | D703-K |
| Catalog Number | D703-K |
| Company DUNS | 009900424 |
| Company Name | PARKELL, INC. |
| 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 | 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810000520107 [Primary] |
FDA Product Code
| EKZ | Unit, Electrosurgical, And Accessories, Dental |
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 | 2021-12-22 |
| Device Publish Date | 2021-12-10 |
On-Brand Devices [Sensimatic™]
| 00810000520770 | Indifferent Plate and Cable for SSensimatic® 700SE |
| 00810000520763 | Electrode Handpiece and Cable for Sensimatic® 700SE |
| 00810000520756 | D700SE Sensimatic™ Electrosurge 230volts |
| M595D6330 | Black Handpiece and Cable for Sensimatic® Electrosurge |
| M595D633CK0 | Locking Chuck (only) for Sensimatic™ Handpiece |
| M595D700SE1100 | D700SE Sensimatic™ Electrosurge 110v |
| M595D6340 | Indifferent Plate for Sensimatic™ Electrosurge |
| M595D6010 | New Indifferent Plate & Red Cable for Sensimatic™ 600SE (Complies with New FDA Lead Wire Regul |
| 00810000520107 | Indifferent Plate and Cable for Sensimatic® 700SE (Korea) |
| M595D700SE10CR0 | Certified Refurbish 700SE Sensimatic™ Electrosurge 110 Volt |
| M595D600SE1100 | D600SE Sensimatic™ Electrosurge 110 Volt |
Trademark Results [Sensimatic]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SENSIMATIC 87217477 5214026 Live/Registered |
Parkell, Inc. 2016-10-27 |
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