Identity
- Trade Name
- OSSEOUS Jobson Horne Probe-Oval 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
- EI0963 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
- 08906039319637 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 — 152 Millimeter FDA UDILength — 2.80 Millimeter FDA UDIWidth — 1.34 Millimeter FDA UDI
Category: Abdominal/ENT/orthopaedic surgical probe, single-use
OSSEOUS Jobson Horne Probe-Oval 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.
- Insertion Probe L — Med-El Elektromedizinische Geräte Gesellschaft m.b.H. · Class III
- Insertion Probe — Med-El Elektromedizinische Geräte Gesellschaft m.b.H. · Class III
- Susol® Probe Jobson-Horne 18cm (Pack of 25) Non Sterile — BAILEY INSTRUMENTS LTD · Class I
- Formby Cerumen Hook & Probe, 178mm — DTR MEDICAL LIMITED · Class I
- OSSEOUS Jobson Horne Probe-Round — EON MEDITECH PRIVATE LIMITED · Class I
- OSSEOUS Cerumen hook — EON MEDITECH PRIVATE LIMITED · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Eon Meditech Private Limited
Sources (1)
- FDA UDI a9677356-ba35-4a53-85e0-89c58c894cb6 35 fields · synced May 30, 2026