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Doubleflo

FDA UDI

Class II (US FDA UDI)

by Hemodia

Identity

Trade Name
DOUBLEFLO FDA UDI
Generic Name
Arthroscopic irrigation/insufflation system FDA UDI
Device Name
DOUBLEFLO INFLOW/OUTFLOW PUMP - Retrofit FDA UDI
Model / Reference
B1 FDA UDI
Description
DOUBLEFLO INFLOW/OUTFLOW PUMP - Retrofit FDA UDI

Identifiers

Catalog Number
72205776F FDA UDI
Primary DI / UDI-DI
03661379239056 FDA UDI
510(k) Number
K221919 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Arthroscopic irrigation/insufflation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Arthroscopic irrigation/insufflation system

Doubleflo by Hemodia — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic irrigation/insufflation system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hemodia

Sources (1)

  • FDA UDI a3c2f64e-9f39-4030-b2dc-5b4f3497a117 35 fields · synced May 31, 2026