Identity
- Trade Name
- pH Electrode FDA UDI
- Generic Name
- Laboratory pH electrode FDA UDI
- Model / Reference
- AV-BP9401D FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00811403010370 FDA UDI
- GMDN Term
- Laboratory pH electrode FDA UDI
Classification
- 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
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laboratory pH electrode
pH Electrode by DIAMOND DIAGNOSTICS Inc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Laboratory pH electrode.
- pH Electrode — Roche Diagnostics Corp. · Class II
- pH Electrode — Medica Corp. · Class II
- Ready Sensor™ Glucose Biosensor — Siemens Healthcare Diagnostics · Class II
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- DIAMOND DIAGNOSTICS Inc
Sources (1)
- FDA UDI ccf8da8f-7e88-42d6-aa5a-a1fe44335fcd 32 fields · synced May 29, 2026