Identity
- Trade Name
- Anmuth Medical International FDA UDI
- Generic Name
- Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
- Device Name
- Grooved Director Buttoned 14.5cm/5.5" FDA UDI
- Model / Reference
- 26-112-14 FDA UDI
- Description
- Grooved Director Buttoned 14.5cm/5.5" FDA UDI
Identifiers
- Catalog Number
- 26-112-14 FDA UDI
- Primary DI / UDI-DI
- 08403207004420 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Dimensions & Sizes
- Size
- Length — 5.5 Inch FDA UDI
Category: Abdominal/ENT/orthopaedic surgical probe, reusable
A reusable, rod-like, hand-held manual surgical instrument designed for exploring cavities, wounds or fistulas during various surgical interventions in the abdominal, ENT, and/or orthopaedic specialties. Made of rigid or flexible metallic and/or synthetic polymer material, it is a single- or double-ended device with various tip configurations.
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Authorization Coverage (1 country)
Regulatory Authorizations
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
- Anmuth Medical International Llc
Sources (1)
- FDA UDI c603b42e-a14c-4b1b-bff6-3b6372484269 36 fields · synced Jul 25, 2026