Identity
- Trade Name
- Manifold FDA UDI
- Generic Name
- Fluid transfer set, general-purpose FDA UDI
- Device Name
- 2 Port Manifold - Right/Off/Block Body - 500 PSI FDA UDI
- Model / Reference
- 193111 FDA UDI
- Description
- 2 Port Manifold - Right/Off/Block Body - 500 PSI FDA UDI
Identifiers
- Catalog Number
- 193111 FDA UDI
- Primary DI / UDI-DI
- 00886333207008 FDA UDI
- 510(k) Number
- K915301 FDA UDI
- FDA Product Code
- DTL FDA UDI
- GMDN Term
- Fluid transfer set, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4290 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Fluid transfer set, general-purpose
Manifold by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Argon Medical Devices, Inc.
Sources (1)
- FDA UDI e61d4cd6-8b7d-49d3-9993-b530de19dbae 37 fields · synced Jun 9, 2026