Identity
- Trade Name
- Med-Dyne FDA UDI
- Generic Name
- Neonatal multi-parameter bedside monitor FDA UDI
- Device Name
- REUSABLE BLACK CARBON ELECTRODE - PACK OF 20 (SINGLE PATIENT USE) FDA UDI
- Model / Reference
- REL1000-20 FDA UDI
- Description
- REUSABLE BLACK CARBON ELECTRODE - PACK OF 20 (SINGLE PATIENT USE) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817497021476 FDA UDI
- FDA Product Code
- DRX FDA UDI
- GMDN Term
- Neonatal multi-parameter bedside monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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: Neonatal multi-parameter bedside monitor
Med-Dyne by Med-Dyne — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- VS Cap Small — Surepulse Medical Limited · Class II
- Med-Dyne — MED-DYNE · 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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Med-Dyne
Sources (1)
- FDA UDI c64abab0-34bd-4cb2-8fd9-12f42936fb5c 34 fields · synced May 30, 2026