Identity
- Trade Name
- ENDOPRO IQ FDA UDI
- Generic Name
- Radiology information system FDA UDI
- Device Name
- NURSING NOTES FDA UDI
- Model / Reference
- M70214-UP FDA UDI
- Description
- NURSING NOTES FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04961333243679 FDA UDI
- FDA Product Code
- OUG FDA UDI
- GMDN Term
- Radiology information system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6310 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Radiology information system
Explore the Endopro IQ medical device, a dedicated computerized radiology information system (RIS) designed to support healthcare facilities in their administrative and clinical activities.
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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 e27f1f7f-b1ff-4f5d-9d7c-fc4db505bf09 33 fields · synced Jun 24, 2026