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Endo-Flo

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
Endo-Flo FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Endo-Flo Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 5mm x 33cm Probe Tip, and Cojoined Suction and Irrigation Tubing FDA UDI
Model / Reference
0025521 FDA UDI
Description
Endo-Flo Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 5mm x 33cm Probe Tip, and Cojoined Suction and Irrigation Tubing FDA UDI

Identifiers

Catalog Number
0025521 FDA UDI
Primary DI / UDI-DI
00801741065200 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

Yes

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 — 33 Centimeter FDA UDI
Outer Diameter — 5 Millimeter FDA UDI

Category: Surgical irrigation/aspiration cannula, non-illuminating, single-use

Endo-Flo by Davol Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI a629ac9f-45a0-404d-b0f2-1b5c9c2cd560 37 fields · synced Jun 6, 2026