Covidien 33135
by Hygia Health Services, Inc.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10817357020257 | Date30 Sep 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Covidien
- Generic Name
- Electrocardiographic lead set, reprocessed
- Model / Reference
- 33135
- Primary DI / UDI-DI
- 10817357020257
- FDA Product Code
- IKD
- GMDN Term
- Electrocardiographic lead set, reprocessed
- Device Class
- Class II
- Regulation Number
- 890.1175
- GUDID distribution status
- Not in Commercial Distribution
Other devices from Hygia Health Services, Inc.
Properties
Other properties (9)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No