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Namic

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
NAMIC FDA UDI
Generic Name
Invasive-pressure external transducer, single-use FDA UDI
Device Name
MANIFOLD 4V COMP. RH/ON PG FDA UDI
Model / Reference
70058408 FDA UDI
Description
MANIFOLD 4V COMP. RH/ON PG FDA UDI

Identifiers

Catalog Number
70058408 FDA UDI
Primary DI / UDI-DI
10193489065800 FDA UDI
FDA Product Code
DRS FDA UDI
GMDN Term
Invasive-pressure external transducer, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2850 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

No

FDA UDI

Category: Invasive-pressure external transducer, single-use

Namic by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive-pressure external transducer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 5a066300-b7c0-44dd-a809-4819fd8244c6 35 fields · synced Jun 1, 2026