FDA UDI In Commercial Distribution 🇺🇸 United States

Tasso+

DI: 00850038691004 · Model: K1013-01 · Tasso, Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Tasso+
Primary DI
00850038691004
Version / Model
K1013-01
Company Name
Tasso, Inc
Labeler DUNS
078431936
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-21
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
06072da4-7fba-4fa2-b89c-ec3d8e4f58f9

Device Description

The Tasso+ is a single-use blood lancing device intended for obtaining microliter capillary whole blood samples.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
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
Yes
Sterilization Methods
Radiation Sterilization

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 10850038691001
Primary 00850038691004

Customer Contacts

Phone
800-257-2370

Premarket Submissions

Submission Number Supplement Number
K221131 000