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OSSEOUS Cerumen hook

FDA UDI

Class I (US FDA UDI)

by Eon Meditech Private Limited

Identity

Trade Name
OSSEOUS Cerumen hook FDA UDI
Generic Name
Abdominal/ENT/orthopaedic surgical probe, single-use FDA UDI
Device Name
"Jobson Horne Probe and Cerumen hook are used to hook out wax or foreign bodies from the ear canal. " FDA UDI
Model / Reference
EI0964 FDA UDI
Description
"Jobson Horne Probe and Cerumen hook are used to hook out wax or foreign bodies from the ear canal. " FDA UDI

Identifiers

Primary DI / UDI-DI
08906039319644 FDA UDI
FDA Product Code
JYG FDA UDI
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, 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
Length — 135 Millimeter FDA UDI
Outer Diameter — 1 Millimeter FDA UDI
Outer Diameter — 2.10 Millimeter FDA UDI

Category: Abdominal/ENT/orthopaedic surgical probe, single-use

OSSEOUS Cerumen hook by Eon Meditech Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal/ENT/orthopaedic surgical probe, 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 f8572bed-a145-4413-8ede-048946031e77 35 fields · synced May 30, 2026