Identity
- Trade Name
- Yumizen C1200 Magnesium FDA UDI
- Generic Name
- Magnesium (Mg2+) IVD, kit, spectrophotometry FDA UDI
- Model / Reference
- 1300023859 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03610230007112 FDA UDI
- 510(k) Number
- K060205 FDA UDI
- FDA Product Code
- JGJ FDA UDI
- GMDN Term
- Magnesium (Mg2+) IVD, kit, spectrophotometry FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1495 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
No
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: Magnesium (Mg2+) IVD, kit, spectrophotometry
Yumizen C1200 Magnesium by Horiba Abx — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Horiba Abx
Sources (1)
- FDA UDI 3e8ff21b-0a0f-432b-a797-cebe9871c83e 33 fields · synced Jun 8, 2026