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ICU Medical

FDA UDI

Class II (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name
ICU Medical FDA UDI
Generic Name
In-line backflow valve, single-use FDA UDI
Device Name
2 Gang 1o2™ Manifold (Red, Blue), Rotating Luer FDA UDI
Model / Reference
SMV52 FDA UDI
Description
2 Gang 1o2™ Manifold (Red, Blue), Rotating Luer FDA UDI

Identifiers

Catalog Number
SMV52 FDA UDI
Primary DI / UDI-DI
00887709042117 FDA UDI
510(k) Number
K974589 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
In-line backflow valve, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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: In-line backflow valve, single-use

ICU Medical by Icu Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as In-line backflow valve, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icu Medical, Inc.

Sources (1)

  • FDA UDI 2483854e-6246-4441-9019-744a7b4bf715 36 fields · synced May 30, 2026