Identity
- Trade Name
- AboutTime MPD 21Gx 1.8mm Safety Lancet FDA UDI
- Generic Name
- Manual blood lancing device, single-use FDA UDI
- Device Name
- 21G x 1.8mm MPD Safety Lancet Box of 100 Single use Sterile Safe Needle is fully shielded before and after use Sterilized by gamma irradiation Comfortable High Quality Tri-bevel point with high speed penetration Tri-Bevel tip ensures good blood flow Optimal ergonomic design Convenient Pre-loaded and pressure activated device Less pressure power. FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 21G x 1.8mm MPD Safety Lancet Box of 100 Single use Sterile Safe Needle is fully shielded before and after use Sterilized by gamma irradiation Comfortable High Quality Tri-bevel point with high speed penetration Tri-Bevel tip ensures good blood flow Optimal ergonomic design Convenient Pre-loaded and pressure activated device Less pressure power. FDA UDI
Identifiers
- Catalog Number
- P1452 FDA UDI
- Primary DI / UDI-DI
- 00628465014525 FDA UDI
- FDA Product Code
- FMK FDA UDI
- GMDN Term
- Manual blood lancing device, 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual blood lancing device, single-use
AboutTime MPD 21Gx 1.8mm Safety Lancet by Medical Plastic Devices M.P.D. 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
- Medical Plastic Devices M.P.D. Inc
Sources (1)
- FDA UDI 23e5e35e-f58f-4368-8f69-c801a234dfb5 34 fields · synced May 30, 2026