Identity
- Trade Name
- AE II BAN FDA UDI
- Generic Name
- Breathing mouthpiece, reusable FDA UDI
- Model / Reference
- Filtered Mouthpiece, cs/50 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00604351600508 FDA UDI
- FDA Product Code
- BYW FDA UDI
- GMDN Term
- Breathing mouthpiece, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5675 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ae Ii Ban by Monaghan Medical Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Monaghan Medical Corp.
Sources (1)
- FDA UDI 6da4fca0-9cbb-4645-a9af-798f409440ce 34 fields · synced Jun 6, 2026