FDA UDI In Commercial Distribution 🇺🇸 United States

microdot®

DI: 00847713000060 · Model: 523-23 · Cambridge Sensors USA LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
microdot®
Primary DI
00847713000060
Version / Model
523-23
Company Name
Cambridge Sensors USA LLC
Labeler DUNS
962314360
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2023-01-10
Public Version
1
Public Version Date
2023-01-18
Public Version Status
New
Public Device Record Key
dfec750f-c8ed-472b-ae66-f8cf46c0e259

Device Description

23g /2.2mm Pressure Activated Safety Lancet (Box of 200 lancets)

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Primary 00847713000060
Package 00847713000152
Unit of Use 00847713000329

Premarket Submissions

Submission Number Supplement Number
K222376 000