Identity
- Trade Name
- ReliOn safety lancet FDA UDI
- Generic Name
- Blood lancet, single-use FDA UDI
- Device Name
- Safety lancets are sterile, single use medical devices intended for capillary blood sampling. Intendent users are healthcare professionals and lay users. FDA UDI
- Model / Reference
- 30G 1.5mm FDA UDI
- Description
- Safety lancets are sterile, single use medical devices intended for capillary blood sampling. Intendent users are healthcare professionals and lay users. FDA UDI
Identifiers
- Catalog Number
- 8601 FDA UDI
- Primary DI / UDI-DI
- 00681131133470 FDA UDI
- FDA Product Code
- FMK FDA UDI
- GMDN Term
- Blood lancet, single-use 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
Category: Blood lancet, single-use
ReliOn safety lancet by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Blood lancet, single-use.
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- DropSafe Medlance Plus, safety lancets — HTL STREFA S A · Class II
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
- Walmart Stores
Sources (1)
- FDA UDI 5124356e-c7bb-4a1f-a205-2aae1bf3a673 34 fields · synced May 30, 2026