Identity
- Trade Name
- Diagnostix™ FDA UDI
- Generic Name
- Aneroid manual sphygmomanometer FDA UDI
- Device Name
- DIAGNOSTIX Aneroid Sphyg,Adult, Orange, LF FDA UDI
- Model / Reference
- 778-11AOR FDA UDI
- Description
- DIAGNOSTIX Aneroid Sphyg,Adult, Orange, LF FDA UDI
Identifiers
- Catalog Number
- 778-11AOR FDA UDI
- Primary DI / UDI-DI
- 00634782067823 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Aneroid manual sphygmomanometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 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
Yes
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
Yes
FDA UDI
Category: Aneroid manual sphygmomanometer
Diagnostix™ by American Diagnostic Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- American Diagnostic Corporation
Sources (1)
- FDA UDI 1ab976d2-92af-4979-b5d3-345e7aa28b6e 37 fields · synced Jun 8, 2026