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Zyno Solutions

FDA UDI

Class II (US FDA UDI)

by Optumhealth Care Solutions, Inc.

Identity

Trade Name
Zyno Solutions FDA UDI
Generic Name
Ambulatory non-insulin infusion pump, electronic FDA UDI
Device Name
Nimbus II-Optum Homecare Infusion FDA UDI
Model / Reference
Pump Nimbus II Plus FDA UDI
Description
Nimbus II-Optum Homecare Infusion FDA UDI

Identifiers

Catalog Number
AAA-00170 FDA UDI
Primary DI / UDI-DI
00862492000308 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Ambulatory non-insulin infusion pump, electronic 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ambulatory non-insulin infusion pump, electronic

Zyno Solutions by Optumhealth Care Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory non-insulin infusion pump, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb3da3a2-6829-4887-9fd6-c2fa5982a168 34 fields · synced Jun 8, 2026