Identity
- Trade Name
- OneTouch Ultrasoft FDA UDI
- Generic Name
- Glucose monitoring system IVD, point-of-care FDA UDI
- Device Name
- OneTouch Ultrasoft Lancets FDA UDI
- Model / Reference
- 020-393 FDA UDI
- Description
- OneTouch Ultrasoft Lancets FDA UDI
Identifiers
- Catalog Number
- 020-393 FDA UDI
- Primary DI / UDI-DI
- 00353885393102 FDA UDI
- FDA Product Code
- FMK FDA UDI
- GMDN Term
- Glucose monitoring system IVD, point-of-care FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4850 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Dimensions & Sizes
- Size
- Needle Gauge — 28 Gauge FDA UDI
Category: Glucose monitoring system IVD, point-of-care
OneTouch Ultrasoft by Lifescan Europe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Lifescan Europe
Sources (1)
- FDA UDI 47e52ab8-a893-430b-8a9d-8f0bcd4c6b71 36 fields · synced Jun 8, 2026