Identity
- Trade Name
- Diagnostix™ FDA UDI
- Generic Name
- Ophthalmic/otologic diagnostic set FDA UDI
- Device Name
- Adstation Oto+-L/Coax+Oph-X,Clock Aner, EU FDA UDI
- Model / Reference
- 56802A-7EU FDA UDI
- Description
- Adstation Oto+-L/Coax+Oph-X,Clock Aner, EU FDA UDI
Identifiers
- Catalog Number
- 56802A-7EU FDA UDI
- Primary DI / UDI-DI
- 00634782088835 FDA UDI
- FDA Product Code
- ERA FDA UDIHLJ FDA UDIDXQ FDA UDI
- GMDN Term
- Ophthalmic/otologic diagnostic set FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4770 FDA UDI886.1570 FDA UDI870.1120 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
Yes
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 sphygmomanometerOphthalmic/otologic diagnostic set
Diagnostix™ by American Diagnostic Corporation — 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
- American Diagnostic Corporation
Sources (1)
- FDA UDI aee1cdb5-27f3-4ffa-b2a8-b26604e36bf8 36 fields · synced Jun 1, 2026