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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Intravenous pressure infusor, automated FDA UDI
Device Name
Infuser Compressor 110V 60 Hz FDA UDI
Model / Reference
270179 FDA UDI
Description
Infuser Compressor 110V 60 Hz FDA UDI

Identifiers

Catalog Number
270179 FDA UDI
Primary DI / UDI-DI
30653405048026 FDA UDI
510(k) Number
K990447 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Intravenous pressure infusor, automated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous pressure infusor, automated

Conmed by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous pressure infusor, automated.

Cleared under the same submission

K990447 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI f50f4776-344a-4697-bc1c-49102cf518de 37 fields · synced Jun 8, 2026