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Infuset™ Gp

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
INFUSET™ GP FDA UDI
Generic Name
Irrigation syringe FDA UDI
Device Name
INFUSET™ GP GENERAL PURPOSE SOLUTION DELIVERY SYSTEM FDA UDI
Model / Reference
59-5014 FDA UDI
Description
INFUSET™ GP GENERAL PURPOSE SOLUTION DELIVERY SYSTEM FDA UDI

Identifiers

Primary DI / UDI-DI
60888937015975 FDA UDI
FDA Product Code
KYZ FDA UDI
GMDN Term
Irrigation syringe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6960 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Irrigation syringe

Infuset™ Gp by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Irrigation syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d3b7aeb8-f041-4760-baad-313fc1ea5775 33 fields · synced Jun 9, 2026