Identity
- Trade Name
- MULTIFLOW FDA UDI
- Generic Name
- Patient monitoring system module, electrocardiographic/respiratory FDA UDI
- Device Name
- DUAL NO CASING RESP. MONITOR FDA UDI
- Model / Reference
- SM-602353 FDA UDI
- Description
- DUAL NO CASING RESP. MONITOR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849593015585 FDA UDI
- FDA Product Code
- BZQ FDA UDI
- GMDN Term
- Patient monitoring system module, electrocardiographic/respiratory FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.2375 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Patient monitoring system module, electrocardiographic/respiratory
Multiflow by Advantage Medical Electronics, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient monitoring system module, electrocardiographic/respiratory.
- Welch Allyn, Inc. — Welch Allyn, Inc. · Class II
- ULTRAFLOW — Advantage Medical Electronics, LLC · Class II
- MULTIFLOW — Advantage Medical Electronics, LLC · 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
- Advantage Medical Electronics, LLC
Sources (1)
- FDA UDI 5f357ee0-2dfb-41cc-b457-da8244aa6a6b 34 fields · synced May 30, 2026