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OSSEOUS Suction Tube - Fine Tip

FDA UDI

Class I (US FDA UDI)

by Eon Meditech Private Limited

Identity

Trade Name
OSSEOUS Suction Tube - Fine Tip FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Suction tubes fine tip are used for suction of fluid and other media from the ear in micro level. FDA UDI
Model / Reference
EI1504 FDA UDI
Description
Suction tubes fine tip are used for suction of fluid and other media from the ear in micro level. FDA UDI

Identifiers

Primary DI / UDI-DI
08904428724055 FDA UDI
FDA Product Code
JZF FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.4 Millimeter FDA UDI
Length — 40.5 Millimeter FDA UDI

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

OSSEOUS Suction Tube - Fine Tip by Eon Meditech Private Limited — Class I — 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
Eon Meditech Private Limited

Sources (1)

  • FDA UDI 10416809-c885-4809-8d3a-f93bb3814384 35 fields · synced May 30, 2026