Identity
- Trade Name
- Merit® Manifold FDA UDI
- Generic Name
- Stopcock FDA UDI
- Model / Reference
- 00884450022399 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884450022399 FDA UDI
- FDA Product Code
- DQO FDA UDI
- GMDN Term
- Stopcock FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1200 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
No
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
No
FDA UDI
Category: Stopcock
The Merit Manifold is a general-purpose valve used to regulate the direction of a liquid or gas flow in medical devices, such as intravenous lines. It is typically constructed of durable materials and may be used for various purposes, including cardiovascular and diagnostic procedures.
Similar devices
Also classified as Stopcock.
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Merit Medical Systems, Inc.
Sources (1)
- FDA UDI adaf6c7b-7ec3-4a0b-9824-dd3ac6d6bd78 33 fields · synced Jul 12, 2026