RESPIRONICS 1041200
GUDID 20653405000836
ECG LEAD SET, 5-WIRE, INTERNATIONAL, 30 IN. (76 CM)
Conmed Corporation
Electrocardiographic lead set, reusable| Primary Device ID | 20653405000836 |
| NIH Device Record Key | 0ea58627-b0c1-4b3c-9f47-7fac002b2bed |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RESPIRONICS |
| Version Model Number | 1041200 |
| Catalog Number | 1041200 |
| 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
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20653405000836 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K933649
FDA Product Code
| DSA | CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [RESPIRONICS]
| 20653405000836 | ECG LEAD SET, 5-WIRE, INTERNATIONAL, 30 IN. (76 CM) |
| 20653405000829 | ECG LEAD SET, 5-WIRE. DOMESTIC, 30 IN. (76 CM) |
Trademark Results [RESPIRONICS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RESPIRONICS 90374954 not registered Live/Pending |
PHILIPS RS NORTH AMERICA LLC 2020-12-11 |
 RESPIRONICS 79299775 not registered Live/Pending |
Koninklijke Philips N.V. 2020-11-04 |
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