Identity
- Trade Name
- CareLiving Safety Lancet 30 FDA UDI
- Generic Name
- Manual blood lancing device, single-use FDA UDI
- Device Name
- Safety lancet 30G*1.8mm,100 Sterile Tip Lancets Per Box,One Handed Use,No Lancing Device Required,Automic Needle Retraction,Lock out after use is a Safety Feature That Negates Needle stick injuries And Prevents Blood cross-contamination FDA UDI
- Model / Reference
- Safety Lancet 30 FDA UDI
- Description
- Safety lancet 30G*1.8mm,100 Sterile Tip Lancets Per Box,One Handed Use,No Lancing Device Required,Automic Needle Retraction,Lock out after use is a Safety Feature That Negates Needle stick injuries And Prevents Blood cross-contamination FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00383568100222 FDA UDI
- GMDN Term
- Manual blood lancing device, single-use FDA UDI
Classification
- 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
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 30 Gauge FDA UDI
Category: Manual blood lancing device, single-use
CareLiving Safety Lancet 30 by Care Living Diagnostics Inc — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Care Living Diagnostics Inc
Sources (1)
- FDA UDI ca2c9eef-86fb-47b0-8656-a4df555cb5d8 34 fields · synced Jun 8, 2026