FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040029043 · Model: 9007991 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Henry Schein
Primary DI
10304040029043
Version / Model
9007991
Catalog Number
9007991
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
281052e5-0b4e-42f4-89ce-edee878fc56b

Device Description

Lancet Safety Press Act Purple

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
Yes
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
FMK LANCET, BLOOD

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Package 20304040029040
Primary 10304040029043
Unit of Use 00304040029046

Device Sizes

Type Value Unit Text
Depth 1.8 Millimeter
Device Size Text, specify Needle Gauge:0.36mm

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
0 – 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
devices kept at room temperature