Identity
- Trade Name
- Ultracell® FDA UDI
- Generic Name
- Ear wick, non-biodegradable FDA UDI
- Device Name
- ***NON-STERILE*** SHIPPERT MED FENESTRATED EAR WICK, 9MM DIA X 15MM (250/SP) FDA UDI
- Model / Reference
- SM-NS30305-C FDA UDI
- Description
- ***NON-STERILE*** SHIPPERT MED FENESTRATED EAR WICK, 9MM DIA X 15MM (250/SP) FDA UDI
Identifiers
- Catalog Number
- SM-NS30305-C FDA UDI
- Primary DI / UDI-DI
- 30886158014783 FDA UDI
- 510(k) Number
- K920357 FDA UDI
- FDA Product Code
- KCN FDA UDI
- GMDN Term
- Ear wick, non-biodegradable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.5220 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ear wick, non-biodegradable
Ultracell® by Beaver-Visitec International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K920357 also covers:
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
- Beaver-Visitec International, Inc.
Sources (1)
- FDA UDI 7ce7c128-2c6b-4cca-af2a-66ae9b28b492 37 fields · synced May 30, 2026