Identity
- Trade Name
- Elecsys hGH FDA UDI
- Generic Name
- Human growth hormone (HGH) IVD, kit, chemiluminescent immunoassay FDA UDI
- Model / Reference
- 5390125190 FDA UDI
Identifiers
- Catalog Number
- 5390125190 FDA UDI
- Primary DI / UDI-DI
- 04015630926664 FDA UDI
- FDA Product Code
- CFL FDA UDI
- GMDN Term
- Human growth hormone (HGH) IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1370 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Human growth hormone (HGH) IVD, kit, chemiluminescent immunoassay
Elecsys hGH by Roche Diagnostics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Elecsys hGH — Roche Diagnostics Corp. · Class I
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
- Roche Diagnostics Corp.
Sources (1)
- FDA UDI 213d0d7c-8fd3-4d22-ba89-7cf5561ec99d 33 fields · synced May 30, 2026