Resscan 22203
Resscan 22203 is a Class II device made by Resmed Pty Ltd, listed in FDA GUDID since 13 Sep 2016 (UDI-DI 00619498222032), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00619498222032 | Date13 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00619498222032
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Resscan
- Generic name
- Ventilator application software
- Model / Ref / Catalog
- 22203
- Primary DI / UDI-DI
- 00619498222032
- FDA product code
- BZD
- GMDN term
- Ventilator application software
- Device class
- Class II
- Regulation number
- 868.5905
- GUDID distribution status
- In Commercial Distribution
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