FDA UDI In Commercial Distribution 🇺🇸 United States

ReadyLance

DI: 00732671008015 · Model: 801 · AMITY HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
ReadyLance
Primary DI
00732671008015
Version / Model
801
Catalog Number
801
Company Name
AMITY HOLDINGS, LLC
Labeler DUNS
016069284
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-08-27
Public Version
1
Public Version Date
2020-09-04
Public Version Status
New
Public Device Record Key
43b70a35-eb16-46aa-8f32-278d74c34148
Distribution End Date
2025-08-27

Device Description

Safety Lancet

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
61579 Blood lancet, single-use

Identifiers

Type ID
Package 20732671208013
Primary 00732671008015
Unit of Use 10732671108019
Package 30732671308017

Customer Contacts

Phone
8003278894

Device Sizes

Type Value Unit Text
Needle Gauge 30 Gauge
Length 1.0 Millimeter