Identity
- Trade Name
- ACCU-CHEK GUIDE LINK FDA UDI
- Generic Name
- Glucose analyser IVD, home-use FDA UDI
- Device Name
- ACCU-CHEK GUIDE LINK MG/DL 118 FDA UDI
- Model / Reference
- 08109257002 FDA UDI
- Description
- ACCU-CHEK GUIDE LINK MG/DL 118 FDA UDI
Identifiers
- Catalog Number
- 08109257002 FDA UDI
- Primary DI / UDI-DI
- 00365702702417 FDA UDI
- PMA Number
- P160017 FDA UDI
- FDA Product Code
- OZP FDA UDI
- GMDN Term
- Glucose analyser IVD, home-use FDA UDI
Classification
- Device Class
- Class III 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Glucose analyser IVD, home-use
Accu-Chek Guide Link by Roche Diagnostics Operations, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Glucose analyser IVD, home-use.
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- telli health — Bioland Technology Ltd. · Class II
- OneTouch Ultra2 — Lifescan Europe · Class II
- iHealth — IHEALTH LAB INC. · Class II
- NuvoMed — NUVOMED INC · Class II
- VivaGuard Ino Smart Blood Glucose Meter — ABOUND Diagnostics, Inc · Class II
Cleared under the same submission
P160017 also covers:
- CONTOUR® NEXT — ASCENSIA DIABETES CARE US INC.
- CONTOUR® NEXT — ASCENSIA DIABETES CARE US INC.
- CONTOUR® NEXT — ASCENSIA DIABETES CARE US INC.
- CONTOUR® NEXT — ASCENSIA DIABETES CARE US INC.
- CONTOUR® NEXT LINK 2.4 — ASCENSIA DIABETES CARE US INC.
- Enlite ® — MEDTRONIC MINIMED, INC.
- Guardian ™ Sensor (3) — MEDTRONIC MINIMED, INC.
- Guardian ™ Sensor (3) — MEDTRONIC MINIMED, INC.
- Guardian ™ Sensor (3) — MEDTRONIC MINIMED, INC.
- Guardian™ 4 — MEDTRONIC MINIMED, INC.
- Guardian™ 4 — MEDTRONIC MINIMED, INC.
- Guardian™ 4 Transmitter — MEDTRONIC MINIMED, INC.
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
- Roche Diagnostics Operations, Inc.
Sources (1)
- FDA UDI afb647eb-6f2f-426b-8828-9322753c4dd3 35 fields · synced May 30, 2026