Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Neurosurgical probe FDA UDI
- Device Name
- MCCULLOCH PROBE SET INCLUDES 1 EACH NL9709-008, NL9710-002, NL9710-003, NL9710-005, NL9715 FDA UDI
- Model / Reference
- NL9730 FDA UDI
- Description
- MCCULLOCH PROBE SET INCLUDES 1 EACH NL9709-008, NL9710-002, NL9710-003, NL9710-005, NL9715 FDA UDI
Identifiers
- Catalog Number
- NL9730 FDA UDI
- Primary DI / UDI-DI
- 10885403086304 FDA UDI
- FDA Product Code
- HAO FDA UDI
- GMDN Term
- Neurosurgical probe FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4535 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 03e55b00-e159-4581-9623-bb1bcec11bb5 36 fields · synced Sep 18, 2026