Identity
- Trade Name
- ELMED FDA UDI
- Generic Name
- ENT surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- 4MM,0 DEG., VIEWING, ELMED EOS-HD PREMIUM SINUS SCOPE WITH STORZ TYPE SLEEVE LOCK, PREMIUM GERMAN MADE OPTICAL LENS SYSTEM, STANDARD TYPE ACMI LIGHT POST WITH WOLF AND STORZ ADAPTER, FULLY AUTOCLAVABLE. FDA UDI
- Model / Reference
- 37400-00 FDA UDI
- Description
- 4MM,0 DEG., VIEWING, ELMED EOS-HD PREMIUM SINUS SCOPE WITH STORZ TYPE SLEEVE LOCK, PREMIUM GERMAN MADE OPTICAL LENS SYSTEM, STANDARD TYPE ACMI LIGHT POST WITH WOLF AND STORZ ADAPTER, FULLY AUTOCLAVABLE. FDA UDI
Identifiers
- Catalog Number
- 37400-00 FDA UDI
- Primary DI / UDI-DI
- 00842180186873 FDA UDI
- FDA Product Code
- LRC FDA UDI
- GMDN Term
- ENT surgical procedure kit, non-medicated, reusable 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: ENT surgical procedure kit, non-medicated, reusable
Elmed by Elmed Incorporated — 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
- Elmed Incorporated
Sources (1)
- FDA UDI 31cd4f8f-c939-488b-8a57-c5b1bec69b81 35 fields · synced May 30, 2026