Osseous

FDA UDI

Class I (US FDA UDI)

by Eon Meditech Private Limited

Identity

Trade Name: OSSEOUS FDA UDI
Generic Name: ENT suction dissector FDA UDI
Device Name: Suction tubes for Nose Reusable are used during Rhinology and evacuate liquid from nasal cavities. FDA UDI
Model / Reference: EI1320120L FDA UDI
Description: Suction tubes for Nose Reusable are used during Rhinology and evacuate liquid from nasal cavities. FDA UDI

Identifiers

Primary DI / UDI-DI: 08906039314564 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

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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 2.0 Millimeter FDA UDI
Length — 120.0 Millimeter FDA UDI
Angle — 30 degree FDA UDI

Category: ENT suction dissector

Osseous 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 df81160b-98de-476b-b033-6200e08bd280 35 fields · synced May 30, 2026