Identity
- Trade Name
- NDS FDA UDI
- Generic Name
- Endoscopic video image display unit FDA UDI
- Device Name
- NDS 32" LED DISPLAY, W/O FIBER FDA UDI
- Model / Reference
- NDS90X0619 FDA UDI
- Description
- NDS 32" LED DISPLAY, W/O FIBER FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04961333244539 FDA UDI
- FDA Product Code
- KQM FDA UDI
- GMDN Term
- Endoscopic video image display unit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4160 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 32.0 Inch FDA UDI
Category: Endoscopic video image display unit
Nds by PENTAX of America, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- PENTAX of America, Inc.
Sources (1)
- FDA UDI af79a0d6-da98-43dd-9e81-aa784c9b1e21 34 fields · synced May 31, 2026