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HexaFlow™ Irrigation Pump

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
HexaFlow™ Irrigation Pump FDA UDI
Generic Name
Basic roller pump FDA UDI
Device Name
IRRIGATION PUMP AFR-00005 US PLX FDA UDI
Model / Reference
AFR-00005 FDA UDI
Description
IRRIGATION PUMP AFR-00005 US PLX FDA UDI

Identifiers

Primary DI / UDI-DI
00763000998332 FDA UDI
PMA Number
P240013 FDA UDI
FDA Product Code
OAE FDA UDI
QZI FDA UDI
OAD FDA UDI
GMDN Term
Basic roller pump FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Category: Basic roller pump

HexaFlow™ Irrigation Pump by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic roller pump.

Cleared under the same submission

P240013 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 6799e481-38de-45b7-b411-0d76fef4d5f7 35 fields · synced May 30, 2026