Identity
- Trade Name
- ILO FDA UDI
- Generic Name
- Otoscope, direct FDA UDI
- Device Name
- FullHD Video-Otoscope FDA UDI
- Model / Reference
- Nex-Gen-HDoto FDA UDI
- Description
- FullHD Video-Otoscope FDA UDI
Identifiers
- Catalog Number
- 864-1002 FDA UDI
- Primary DI / UDI-DI
- 04250369709038 FDA UDI
- FDA Product Code
- ERA FDA UDI
- GMDN Term
- Otoscope, direct FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4770 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Otoscope, direct
Ilo by ILO electronic GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- BETA 200 VET. OTOSCOPE — Heine Optotechnik GmbH & Co. KG · Class I
- Firefly — Firefly Global · Class I
- Otoscope — Shenzhen Teslong Technology Co., Ltd · Class I
- Welch Allyn, Inc. — Welch Allyn, Inc. · 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 |
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Manufacturer
- Manufacturer
- ILO electronic GmbH
Sources (1)
- FDA UDI c700b822-5d95-473c-90c9-4f5d45529284 35 fields · synced May 31, 2026