Identity
- Trade Name
- ENDOCAMELEON FDA UDI
- Generic Name
- Arthroscopic access cannula, reusable FDA UDI
- Device Name
- Changing Rod ENDOCAMELEON, cannulated FDA UDI
- Model / Reference
- 28140EWK FDA UDI
- Description
- Changing Rod ENDOCAMELEON, cannulated FDA UDI
Identifiers
- Catalog Number
- 28140EWK FDA UDI
- Primary DI / UDI-DI
- 04048551360231 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Arthroscopic access cannula, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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
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
Category: Arthroscopic access cannula, reusable
Endocameleon by Karl Storz GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Arthroscopic access cannula, reusable.
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- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- INFLOW CANNULA SET — SONTEC INSTRUMENTS, INC. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- OBTURATOR — SONTEC INSTRUMENTS, INC. · Class I
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
- Karl Storz GmbH & Co. KG
Sources (1)
- FDA UDI c12cac4c-9274-46b4-a0e2-893917b2ef8f 35 fields · synced Jun 8, 2026