Nellcor FOAM P/I
by Covidien LP
Ref FOAMP/I
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0763000B000256189 10884522042819 | Date28 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10884522042819 | Date26 Sep 2018 | StatusListed |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Nellcor
- Generic Name
- Adhesive bandage
- Device Name
- Nellcor NS Reusable Sensor Accessories
- Model / Reference
- FOAMP/I EUDAMEDFOAM P/I GUDID
- Primary DI / UDI-DI
- 10884522042819
- Basic UDI-DI
- 0763000B000256189
- FDA Product Code
- KGX
- EMDN Code
- Z1203020485 Gaseous exchange monitoring instruments - consumables
- GMDN Term
- Adhesive bandage
- Device Class
- Class I
- Regulation Number
- 880.5240
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / Reference | FOAMP/I | FOAM P/I |
Other devices from Covidien LP
Properties
Other properties (19)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No