Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- General-purpose absorbent tip applicator/swab, reusable FDA UDI
- Device Name
- UNIVERSITY OF IOWA COTTON APPLICATOR FLAT, PARTIALLY SERRATED TIP OVERALL LENGTH 6" (15.2CM) FDA UDI
- Model / Reference
- RH240 FDA UDI
- Description
- UNIVERSITY OF IOWA COTTON APPLICATOR FLAT, PARTIALLY SERRATED TIP OVERALL LENGTH 6" (15.2CM) FDA UDI
Identifiers
- Catalog Number
- RH240 FDA UDI
- Primary DI / UDI-DI
- 10885403108945 FDA UDI
- FDA Product Code
- KXF FDA UDI
- GMDN Term
- General-purpose absorbent tip applicator/swab, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6025 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 2328e5ab-1777-41ab-aed5-ada43f55930c 36 fields · synced Sep 18, 2026