Identity
- Trade Name
- ERBE FDA UDI
- Generic Name
- Endoscopic cryosurgical probe, reusable FDA UDI
- Device Name
- Flexible cryo probe; for USA OD 2.4mm; L 900mm FDA UDI
- Model / Reference
- 20416-031 FDA UDI
- Description
- Flexible cryo probe; for USA OD 2.4mm; L 900mm FDA UDI
Identifiers
- Catalog Number
- 20416-031 FDA UDI
- Primary DI / UDI-DI
- 04050147007994 FDA UDI
- 510(k) Number
- K051509 FDA UDI
- FDA Product Code
- GEH FDA UDI
- GMDN Term
- Endoscopic cryosurgical probe, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4350 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 900.000 Millimeter FDA UDI
Category: Endoscopic cryosurgical probe, reusable
Erbe by Erbe Elektromedizin GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic cryosurgical probe, reusable.
- ERBE — Erbe Elektromedizin GmbH · Class II
Cleared under the same submission
K051509 also covers:
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
- Erbe Elektromedizin GmbH
Sources (1)
- FDA UDI 1c07c240-078b-473d-8f7e-a726ca0f1b1f 38 fields · synced Jun 8, 2026