Identity
- Trade Name
- HDMD PRO FDA UDI
- Generic Name
- Endoscopic video image processing unit FDA UDI
- Device Name
- HDMD Pro Update the current LiFePO4 Battery 18650 1500mAh-3.2V to LiFePO4 Battery 18650 1800mAh-3.2V FDA UDI
- Model / Reference
- HDMD PRO FDA UDI
- Description
- HDMD Pro Update the current LiFePO4 Battery 18650 1500mAh-3.2V to LiFePO4 Battery 18650 1800mAh-3.2V FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817613021243 FDA UDI
- FDA Product Code
- LMB FDA UDI
- GMDN Term
- Endoscopic video image processing unit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.2010 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
No
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
Yes
FDA UDI
Category: Endoscopic video image processing unit
Hdmd Pro by Nds Surgical Imaging, Llc. — 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
- Nds Surgical Imaging, Llc.
Sources (1)
- FDA UDI 9ac42d9f-4485-4115-a1d0-438b22874003 34 fields · synced May 31, 2026