FDA UDI In Commercial Distribution 🇺🇸 United States

Unistik

DI: 00384700714017 · Model: AT 0714 · OWEN MUMFORD LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
Unistik
Primary DI
00384700714017
Version / Model
AT 0714
Company Name
OWEN MUMFORD LIMITED
Labeler DUNS
217266915
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2020-04-16
Public Version
3
Public Version Date
2023-02-23
Public Version Status
Update
Public Device Record Key
0903cb6c-1c64-422a-94ec-6e7e86ba2355

Device Description

Unistik Extra, 21G x 2.0mm, 200 count - sterile, single use safety lancet

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
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 00384700714031
Primary 00384700714017
Unit of Use 00384700712006

Customer Contacts

Phone
770 977 2226

Device Sizes

Type Value Unit Text
Needle Gauge 21 Gauge
Depth 2.0 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius