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Dexcom G5 Mobile Replacement Receiver Kit
FDA UDIClass III (US FDA UDI)
by Dexcom
Identity
- Trade Name
- Dexcom G5 Mobile Replacement Receiver Kit FDA UDI
- Generic Name
- Percutaneous interstitial fluid glucose monitoring system, electrochemical FDA UDI
- Device Name
- G5 Mobile Replacement Receiver Kit Adult Blue FDA UDI
- Model / Reference
- STR-GF-BLU FDA UDI
- Description
- G5 Mobile Replacement Receiver Kit Adult Blue FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20386270000273 FDA UDI
- PMA Number
- P120005 FDA UDI
- FDA Product Code
- MDS FDA UDI
- GMDN Term
- Percutaneous interstitial fluid glucose monitoring system, electrochemical FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
A comprehensive overview of the Dexcom G5 Mobile Replacement Receiver Kit, including its features and regulatory compliance.
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 III | Pending data |
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Manufacturer
- Manufacturer
- Dexcom
Sources (1)
- FDA UDI 2581bea4-25ae-45f0-9af5-cec5a8520cd5 37 fields · synced Jul 14, 2026