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Infuset-930

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref FP-0010005Model EMED Infuset Flow Control Infusion Set

by EMED Technologies Corporation

Identity

Trade Name
Infuset-930 EUDAMED
Infuset FDA UDI
Generic Name
Mechanical infusion pump administration set FDA UDI
Device Name
Infuset-930, Flow Control Infusion Set EUDAMEDFDA UDI
Model / Reference
EMED Infuset Flow Control Infusion Set EUDAMED
FP-0010005 EUDAMED
Infuset-930 FDA UDI
Description
Infuset-930, Flow Control Infusion set FDA UDI

Identifiers

Catalog Number
FP-0010005 FDA UDI
Primary DI / UDI-DI
00817708020342 EUDAMEDFDA UDI
Basic UDI-DI
B-00817708020342 EUDAMED
510(k) Number
K140133 FDA UDI
FDA Product Code
FPA FDA UDI
EMDN Code
A03010103,A030104 EUDAMED
GMDN Term
Mechanical infusion pump administration set FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 26.36 Centimeter FDA UDI
Total Volume — 0.13 Milliliter FDA UDI

Infuset-930 by EMED Technologies Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000012148
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 4aeefa42-dfdd-4ad3-8988-debf61352d52 61 fields · synced Jun 18, 2026
  • FDA UDI 9a2377e6-491f-4c7d-bb73-f7b1cab218d6 38 fields · synced May 30, 2026