Identity
- Trade Name
- INTL DEMAND VALVE ASSY-CENT.MX FDA UDI
- Generic Name
- Resuscitator face mask, reusable FDA UDI
- Device Name
- INTL DEMAND VALVE ASSY-CENT.MX FDA UDI
- Model / Reference
- 91505092 FDA UDI
- Description
- INTL DEMAND VALVE ASSY-CENT.MX FDA UDI
Identifiers
- Catalog Number
- 91505092 FDA UDI
- Primary DI / UDI-DI
- 00816711024187 FDA UDI
- FDA Product Code
- BYX FDA UDI
- GMDN Term
- Resuscitator face mask, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Resuscitator face mask, reusable
Intl Demand Valve Assy-Cent.mx by Parker Hannifin Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Resuscitator face mask, reusable.
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- FERNO2 — SPIRACLE TECHNOLOGY · Class I
- Rescuer Silicone Resuscitation Mask (#4 Adult) — B.L.S. Systems Limited · Class I
- HUDSON RCI — TELEFLEX INCORPORATED · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Parker Hannifin Corp.
Sources (1)
- FDA UDI a20a53fa-9da5-4109-9b5c-f3b085a53424 34 fields · synced Jun 8, 2026