OSSEOUS Suction Tube for Sinus-Disposable

FDA UDI

Class I (US FDA UDI)

by Eon Meditech Private Limited

Identity

Trade Name: OSSEOUS Suction Tube for Sinus-Disposable FDA UDI
Generic Name: ENT suction dissector FDA UDI
Device Name: Suction tubes for Sinus are used to remove excess amount of foreign body material from sinus. FDA UDI
Model / Reference: EI1840100 FDA UDI
Description: Suction tubes for Sinus are used to remove excess amount of foreign body material from sinus. FDA UDI

Identifiers

Primary DI / UDI-DI: 08904461006842 FDA UDI
FDA Product Code: KAM FDA UDI
GMDN Term: ENT suction dissector FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 100.0 Millimeter FDA UDI
Angle — 30 degree FDA UDI
Outer Diameter — 4.0 Millimeter FDA UDI

Category: ENT suction dissector

OSSEOUS Suction Tube for Sinus-Disposable by Eon Meditech Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Eon Meditech Private Limited

Sources (1)

FDA UDI 17adcaa6-1f13-4c8e-a6fc-379250f3225b 35 fields · synced Jun 8, 2026