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Merit® Manifold

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Merit® Manifold FDA UDI
Generic Name
Stopcock FDA UDI
Model / Reference
00884450312278 FDA UDI

Identifiers

Catalog Number
202LTPHWF-R/D FDA UDI
Primary DI / UDI-DI
00884450312278 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Stopcock 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

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

A general-purpose valve used to regulate the direction of a liquid or gas flow, typically constructed of durable materials and used for various general-purpose purposes. The Merit Manifold is a single-use device that has undergone thorough testing and meets all regulatory requirements.

Similar devices

Also classified as Stopcock.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 26481d44-5196-41a3-ba3f-d7643508a7ec 34 fields · synced Jul 13, 2026