FDA UDI Not in Commercial Distribution 🇺🇸 United States

Tenderlett Finger Incision Device

DI: 20711234308162 · Model: TL100I · ACCRIVA DIAGNOSTICS HOLDINGS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Tenderlett Finger Incision Device
Primary DI
20711234308162
Version / Model
TL100I
Catalog Number
TL100I
Company Name
ACCRIVA DIAGNOSTICS HOLDINGS, INC.
Labeler DUNS
079299318
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2023-03-31
Public Version Status
Update
Public Device Record Key
2d39ae48-1911-41eb-b68d-6fbbcfdd017f
Distribution End Date
2022-11-22

Device Description

Tenderlett Finger Incision Device 100/box

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
Yes
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
61579 Blood lancet, single-use

Identifiers

Type ID
Primary 20711234308162
Unit of Use 00711234308168

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K923302 000

Device Sizes

Type Value Unit Text
Length 0.94 Millimeter
Depth 1.75 Millimeter