Identity
- Trade Name
- Ten20 Conductive Paste FDA UDI
- Generic Name
- Electrode conductive medium FDA UDI
- Device Name
- 3-pack of Ten20 Conductive Paste Single-Use Cups FDA UDI
- Model / Reference
- 10-20-1S FDA UDI
- Description
- 3-pack of Ten20 Conductive Paste Single-Use Cups FDA UDI
Identifiers
- Catalog Number
- 10-20-1S FDA UDI
- Primary DI / UDI-DI
- 30891893002278 FDA UDI
- FDA Product Code
- GYB FDA UDI
- GMDN Term
- Electrode conductive medium FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1275 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrode conductive medium
Ten20 Conductive Paste by D.O. Weaver and Co. — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K883149 | Class II | Active |
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Manufacturer
- Manufacturer
- D.O. Weaver and Co.
- FDA Applicant
- Weaver & Co.
Sources (2)
- FDA UDI 8656f053-3897-4121-8fa4-c812d8ca9d7c 60 fields · synced Jun 18, 2026
- FDA 510(k) K883149 1 fields · synced Jun 4, 2026