FDA UDI Not in Commercial Distribution 🇺🇸 United States

UDI TEST SKU

DI: 17503025060238 · Model: A40401 TST · LIFE TECHNOLOGIES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
UDI TEST SKU
Primary DI
17503025060238
Version / Model
A40401 TST
Company Name
LIFE TECHNOLOGIES CORPORATION
Labeler DUNS
118793157
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2018-06-02
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
6e54e902-9bd0-434e-9052-bee92c790b68
Distribution End Date
2018-06-05

Device Description

UDI TEST SKU Device Description

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FMH CONTAINER, SPECIMEN, STERILE

GMDN Terms

Code Name
36465 General-purpose centrifuge IVD

Identifiers

Type ID
Package 37503025060232
Primary 17503025060238
Unit of Use 87503025060237