Identity
- Trade Name
- Ethox FDA UDI
- Generic Name
- Surgical instrument interim-placement holder, single-use FDA UDI
- Device Name
- ETHOX SK-200N SURG 2 POCKET W/O TAPE - NS FDA UDI
- Model / Reference
- 950089200 FDA UDI
- Description
- ETHOX SK-200N SURG 2 POCKET W/O TAPE - NS FDA UDI
Identifiers
- Catalog Number
- 950089200 FDA UDI
- Primary DI / UDI-DI
- 20889483149727 FDA UDI
- FDA Product Code
- KDD FDA UDI
- GMDN Term
- Surgical instrument interim-placement holder, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Width — 28 Centimeter FDA UDI
Ethox by Ethox Medical, Llc — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ethox Medical, Llc
Sources (1)
- FDA UDI eb4c41f9-65bf-425f-b06a-9205721ed24f 37 fields · synced May 30, 2026