Anesth ID Set Coax WT GSL 210 (BK OD22) MP16052
Ref MP16052Model 2080456K19P030
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0404867512080456K19P030T4 04048675716273 | Date27 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04048675716273 | Date13 Apr 2023 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Anesth ID Set Coax WF GSL 210 (BK OD22) EUDAMEDAnesth ID Set Coax WT GSL 210 (BK OD22) GUDID
- Generic Name
- Anaesthesia breathing circuit, single-use
- Model / Reference
- MP16052, 2080456K19P030
- Primary DI / UDI-DI
- 04048675716273
- Basic UDI-DI
- 0404867512080456K19P030T4
- FDA Product Code
- CAI, BZO
- EMDN Code
- R020102 Coaxial breathing circuits
- GMDN Term
- Anaesthesia breathing circuit, single-use
- Device Class
- Class IIa EUDAMEDClass I GUDID
- Regulation Number
- 868.5240, 868.5975
- EU market of registration
- Germany
- GUDID distribution status
- Not in Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class I |
Other devices from Dragerwerk AG
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
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No