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Orbit soft

FDA UDI

Class II (US FDA UDI)

by Ypsomed AG

Identity

Trade Name
Orbit soft FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
Orbit soft Infusion Set, 9 mm soft cannula, 105 cm (42") blue tubing / An infusion set for infusion pumps with standard Luer-lock connection and 360° rotation. FDA UDI
Model / Reference
O4291OB FDA UDI
Description
Orbit soft Infusion Set, 9 mm soft cannula, 105 cm (42") blue tubing / An infusion set for infusion pumps with standard Luer-lock connection and 360° rotation. FDA UDI

Identifiers

Catalog Number
O4291OB FDA UDI
Primary DI / UDI-DI
07613117016814 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Electric infusion pump administration set, 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

Dimensions & Sizes

Size
Length — 9.0 Millimeter FDA UDI

Category: Electric infusion pump administration set, single-use

Orbit soft by Ypsomed AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric infusion pump administration set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ypsomed AG

Sources (1)

  • FDA UDI ea169b78-6b71-4f74-856b-7e3c214fa3c4 36 fields · synced May 31, 2026