Identity
- Trade Name
- Medline/MMS Sales FDA UDI
- Generic Name
- Non-rebreathing valve, single-use FDA UDI
- Device Name
- MERIDIAN NEXUS FDA UDI
- Model / Reference
- 60301-1 FDA UDI
- Description
- MERIDIAN NEXUS FDA UDI
Identifiers
- Catalog Number
- 60301-1 FDA UDI
- Primary DI / UDI-DI
- 10080196010592 FDA UDI
- FDA Product Code
- CAI FDA UDI
- GMDN Term
- Non-rebreathing valve, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 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
Yes
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Non-rebreathing valve, single-use
Medline/MMS Sales is a non-rebreathing valve designed for single-use anesthesia applications. This device features a unique one-way valve that prevents patient rebreathing of exhaled gases, ensuring optimal breathing gas flow and reducing the risk of patient discomfort.
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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
- Medline Industries, Inc.
Sources (1)
- FDA UDI 8edf88ac-64ec-45cb-9d3e-3e4ff5bd4a18 35 fields · synced Jul 17, 2026