FDA UDI In Commercial Distribution 🇺🇸 United States

Tenderfoot Preemie Heel Stick Device

DI: 20711234302153 · Model: TFP1000I · ACCRIVA DIAGNOSTICS HOLDINGS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1000

Basic Information

Brand Name
Tenderfoot Preemie Heel Stick Device
Primary DI
20711234302153
Version / Model
TFP1000I
Catalog Number
TFP1000I
Company Name
ACCRIVA DIAGNOSTICS HOLDINGS, INC.
Labeler DUNS
079299318
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2023-04-27
Public Version Status
Update
Public Device Record Key
27a8570a-074b-41ae-b9b1-e04678259fc1

Device Description

Tenderfoot Preemie Heel Stick Device 1000/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 Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Primary 20711234302153
Unit of Use 00711234302159

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1.75 Millimeter
Depth 0.85 Millimeter