Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Stopcock FDA UDI
- Device Name
- V. Mueller STOPCOCK FEMALE LUER-LOCK TIP TO MALE LUER-LOCK FDA UDI
- Model / Reference
- HY23152 FDA UDI
- Description
- V. Mueller STOPCOCK FEMALE LUER-LOCK TIP TO MALE LUER-LOCK FDA UDI
Identifiers
- Catalog Number
- HY23152 FDA UDI
- Primary DI / UDI-DI
- 10885403051845 FDA UDI
- FDA Product Code
- DTL FDA UDI
- GMDN Term
- Stopcock FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4290 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 II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 6acdbe38-c7e2-468f-b8d5-85c9582ac0c2 36 fields · synced Sep 18, 2026