Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Intracranial catheter holder FDA UDI
- Device Name
- RIGHT ANGLE GUIDE PED FDA UDI
- Model / Reference
- FV011T FDA UDI
- Description
- RIGHT ANGLE GUIDE PED FDA UDI
Identifiers
- Catalog Number
- FV011T FDA UDI
- Primary DI / UDI-DI
- 04041906118105 FDA UDI
- FDA Product Code
- JXG FDA UDI
- GMDN Term
- Intracranial catheter holder FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5550 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Intracranial catheter holder
Aesculap by Christoph Miethke GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intracranial catheter holder.
- Natus® — Natus Medical Incorporated · Class II
- Natus® — Natus Medical Incorporated · Class II
- Natus® — Natus Medical Incorporated · Class II
- Natus® — Natus Medical Incorporated · Class II
- AESCULAP — Christoph Miethke GmbH & Co. KG · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Christoph Miethke GmbH & Co. KG
Sources (1)
- FDA UDI eca3bb0c-ccdb-432a-9ed5-d7fb476d5fa3 35 fields · synced Jun 8, 2026