Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Tracheal bistoury FDA UDI
- Device Name
- JACKSON TRACHEOTOMIC BISTOURY CURVED WITH BLUNT PROBE POINT OVERALL LENGTH 6-3/4" (17CM) FDA UDI
- Model / Reference
- BE360 FDA UDI
- Description
- JACKSON TRACHEOTOMIC BISTOURY CURVED WITH BLUNT PROBE POINT OVERALL LENGTH 6-3/4" (17CM) FDA UDI
Identifiers
- Catalog Number
- BE360 FDA UDI
- Primary DI / UDI-DI
- 10885403014598 FDA UDI
- FDA Product Code
- KTG FDA UDI
- GMDN Term
- Tracheal bistoury FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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 32813d0f-eb4f-41db-81ac-f334bc771aa5 36 fields · synced Sep 18, 2026