02-Resq 313-7255
02-Resq 313-7255 is a Class II device made by Pulmodyne Inc., listed in FDA GUDID since 12 Feb 2016 (UDI-DI 00841470102951), registry data as of 22 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 | Number00841470102951 | Date12 Feb 2016 | StatusListed |
Official records
- AccessGUDID record 00841470102951
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- 02-Resq
- Generic name
- Respiratory oxygen therapy system
- Model / reference
- 313-7255
- Primary DI / UDI-DI
- 00841470102951
- FDA product code
- BYE
- GMDN term
- Respiratory oxygen therapy system
- Device class
- Class II
- Regulation number
- 868.5965
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Respiratory oxygen therapy system.
- Resusci Flow Rail mounting type 60362 by Atom Medical Corporation
- Resuscitation Unit 104 E type (Stand-alone type) 60982 by Atom Medical Corporation
- AEROSOL MASK, CHILD, SINGLE PACKING OM-82120 by BESMED HEALTH BUSINESS CORP.
- TRACHEOTOMY MASK CHILD, OXYGEN 6mm CONNECTOR OM-81630 by BESMED HEALTH BUSINESS CORP.
- GO-PAP 313-4601N by Pulmodyne Inc.
- GO-PAP 313-4602 by Pulmodyne Inc.