FDA UDI In Commercial Distribution 🇺🇸 United States

Ultilet Safety Blades 21G x 2.2mm

DI: 10743820212259 · Model: 21225 · Boca Med, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
25

Basic Information

Brand Name
Ultilet Safety Blades 21G x 2.2mm
Primary DI
10743820212259
Version / Model
21225
Company Name
Boca Med, LLC
Labeler DUNS
121164730
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2023-04-04
Public Version
1
Public Version Date
2023-04-12
Public Version Status
New
Public Device Record Key
1dee4eae-e0cc-4e0b-aeca-c5cd28baa131

Device Description

Ultilet Safety Blades 21G x 2.2mm HRIC: 08326-2122-25

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
No
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
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
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 20743820212256
Primary 10743820212259
Package 30743820212253
Unit of Use 00743820212252