Identity
- Trade Name
- RUSCH FDA UDI
- Generic Name
- PEEP valve, single-use FDA UDI
- Device Name
- PEEP VALVE 22MM 10/BX FDA UDI
- Model / Reference
- IPN042601 FDA UDI
- Description
- PEEP VALVE 22MM 10/BX FDA UDI
Identifiers
- Catalog Number
- 157200190 FDA UDI
- Primary DI / UDI-DI
- 04026704541911 FDA UDI
- FDA Product Code
- BYE FDA UDI
- GMDN Term
- PEEP valve, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5965 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: PEEP valve, single-use
Rusch by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as PEEP valve, single-use.
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- O2-CPAP — Pulmodyne Inc. · Class II
- AirLife™ — Airlife, Inc. · Class II
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- PEEP VALVE 15cmH2O;STRAIGHT CONNECTORS 30m, 22m — BESMED HEALTH BUSINESS CORP. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 7cfe0042-880c-424e-8dca-e821864c31d0 37 fields · synced Jun 1, 2026