Identity
- Trade Name
- TechLITE® Lancets FDA UDI
- Generic Name
- Blood lancing device tip FDA UDI
- Device Name
- TechLITE Lancets 25g 100's. Load lancet into lancing device and twist off protective cap. Single-use disposable blood lancet should be used for assisted blood draws by healthcare providers or at healthcare provision sites. Dispose of used lancets in approved sharps container. (Primary UPC# 015482880125; Shipper UPC# 015482882549 are used as the assigned UDI for the Class I device.) FDA UDI
- Model / Reference
- 880125 FDA UDI
- Description
- TechLITE Lancets 25g 100's. Load lancet into lancing device and twist off protective cap. Single-use disposable blood lancet should be used for assisted blood draws by healthcare providers or at healthcare provision sites. Dispose of used lancets in approved sharps container. (Primary UPC# 015482880125; Shipper UPC# 015482882549 are used as the assigned UDI for the Class I device.) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00015482880125 FDA UDI
- FDA Product Code
- FMK FDA UDI
- GMDN Term
- Blood lancing device tip 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 — 25 Gauge FDA UDI
Category: Blood lancing device tip
TechLITE® Lancets by Arkray Usa, Inc. — 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
- Arkray Usa, Inc.
Sources (1)
- FDA UDI c52e624d-45fe-424f-81b1-7dbee614abe1 35 fields · synced May 30, 2026