Sidestream 00
by Respironics Respiratory Drug Delivery (UK) Ltd 45 variants
Sidestream 00 (1110824) is a Class II device made by Respironics Respiratory Drug Delivery (UK) Ltd, listed in FDA GUDID since 24 Aug 2016 (UDI-DI 00383730001395), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00383730001395 | Date24 Aug 2016 | StatusListed |
Official records
- AccessGUDID record 00383730001395
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Sidestream
- Generic name
- Therapeutic agent nebulizer, benchtop
- Model / Ref / Catalog
- 00, 1110824
- Primary DI / UDI-DI
- 00383730001395
- FDA product code
- CAF
- GMDN term
- Therapeutic agent nebulizer, benchtop
- Device class
- Class II
- Regulation number
- 868.5630
- GUDID distribution status
- In Commercial Distribution
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