FDA UDI In Commercial Distribution 🇺🇸 United States

SurgiLance Lite Safety Lancet

DI: 38886354702615 · Model: SLL21G220 · MEDIPURPOSE PTE. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
SurgiLance Lite Safety Lancet
Primary DI
38886354702615
Version / Model
SLL21G220
Company Name
MEDIPURPOSE PTE. LTD.
Labeler DUNS
628380248
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2017-01-02
Public Version
4
Public Version Date
2021-11-15
Public Version Status
Update
Public Device Record Key
1dfecb43-3e26-4ed1-ad8e-0c575ab56cf7

Device Description

SurgiLance Lite Safety Lancet, 21G, 2.2mm Lime Green

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 58886354702619
Package 48886354702612
Primary 38886354702615
Unit of Use 18886354702611

Customer Contacts