Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Periodontal curette FDA UDI
- Device Name
- V. Mueller MOLT-TYPE EXODONTIA ORAL CURETTE, NO. 2 OVERALL LENGTH 7" (17.8CM) FDA UDI
- Model / Reference
- MO11019 FDA UDI
- Description
- V. Mueller MOLT-TYPE EXODONTIA ORAL CURETTE, NO. 2 OVERALL LENGTH 7" (17.8CM) FDA UDI
Identifiers
- Catalog Number
- MO11019 FDA UDI
- Primary DI / UDI-DI
- 10885403200458 FDA UDI
- FDA Product Code
- EMK FDA UDI
- GMDN Term
- Periodontal curette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
V. Mueller by Carefusion 2200, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI d815a581-cb18-4b76-b5ec-784e4e59586c 36 fields · synced Sep 18, 2026