FDA UDI In Commercial Distribution 🇺🇸 United States

Acti-Lance, safety lancet

DI: 05901549097023 · Model: Universal, 23G · HTL STREFA S A
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Acti-Lance, safety lancet
Primary DI
05901549097023
Version / Model
Universal, 23G
Catalog Number
7156
Company Name
HTL STREFA S A
Labeler DUNS
422528088
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-05-17
Public Version
1
Public Version Date
2020-05-25
Public Version Status
New
Public Device Record Key
8a1b84d4-95d7-496e-acbb-524959c7038a

Device Description

Safety lancets are sterile, single use medical devices intended for capillary blood sampling. Intended users are healthcare professionals and lay users.

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
61579 Blood lancet, single-use

Identifiers

Type ID
Package 15901549097020
Primary 05901549097023
Unit of Use 85901549097029

Customer Contacts

Phone
+48422700010