FDA Registration
Active
🇨🇦 Canada
989803151641, 12-Lead Complete Lead Set (IEC), Standard Length
Reg #: 3000126629
·
FEI: 3000126629
·
Expires 2025
Products
1
Proprietary Names
13
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- Philips Electronics Ltd
- Registration Number
- 3000126629
- FEI Number
- 3000126629
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 1875 Buckhorn Gate, 5th Floor
- City
- Mississauga Ontario
- Country
- CA
Regulatory Submissions
- 510(k) Number
- K080999
Owner / Operator
- Firm Name
- Philips Medical Systems International BV
- Operator Number
- 1217116
- Address
- Veenpluis 6
- City
- Best
- State
- NL-NOTA
- Postal Code
- 5684PC
- Country
- NL
US Agent
- Business Name
- Philips
- Contact Name
- Shaylee Masilunas
- Address
- 6501 Living Place
- City
- Pittsburgh
- State
- PA
- ZIP
- 15206
- Country
- US
- [email protected]
- Phone
- 724 8162019
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Electrocardiograph | DPS | Class 2 | Cardiovascular | No | 2009-02-03 |
Proprietary Names
989803151641, 12-Lead Complete Lead Set (IEC), Standard Length
989803151761, 15/16/18-Lead Upgrade Kit (IEC), Standard Length
989803151731, 12-Lead Limb Lead Set (AAMI/IEC), Long
989803151651, 12-Lead Complete Lead Set (AAMI), Long
989803151661, 12-Lead Complete Lead Set (IEC), Long
989803164281, USB Patient Data Cable, Class B
989803151751, 15/16/18-Lead Upgrade Kit (AAMI), Standard Length
989803151631, 12-Lead Complete Lead Set (AAMI), Standard Length
989803151771, 15/16/18-Lead Upgrade Kit (AAMI), Long
989803151711, 12-Lead Limb Lead Set (AAMI/IEC), Standard Length
989803151781, 15/16/18-Lead Upgrade Kit (IEC), Long
989803151691, 12-Lead Chest Lead Set (AAMI/IEC), Long
989803151671, 12-Lead Chest Lead Set (AAMI/IEC), Standard Length
Establishment Types
Export Device to the United States But Perform No Other Operation on Device