Identity
- Trade Name
- Earlens Hybrid Impression Kit FDA UDI
- Generic Name
- Earmould impression kit FDA UDI
- Device Name
- Includes - Medial Impression Cartridges - Lateral Impression Cartridges - Medial Mixing Tips - Lateral Mixing Tips FDA UDI
- Model / Reference
- HIK02 FDA UDI
- Description
- Includes - Medial Impression Cartridges - Lateral Impression Cartridges - Medial Mixing Tips - Lateral Mixing Tips FDA UDI
Identifiers
- Catalog Number
- HIK02 FDA UDI
- Primary DI / UDI-DI
- 00850013007349 FDA UDI
- FDA Product Code
- LDG FDA UDI
- GMDN Term
- Earmould impression kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.3300 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
Yes
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
No
FDA UDI
Category: Earmould impression kit
Earlens Hybrid Impression Kit by Earlens Corporation — 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
- Earlens Corporation
Sources (1)
- FDA UDI cde78da9-b57f-4b59-8e18-47678fdc3d4f 35 fields · synced May 30, 2026