FDA UDI In Commercial Distribution 🇺🇸 United States

MICROSAFE®

DI: 05060586450083 · Model: 1020-50 · SAFE-TEC CLINICAL PRODUCTS LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
MICROSAFE®
Primary DI
05060586450083
Version / Model
1020-50
Catalog Number
1020-50
Company Name
SAFE-TEC CLINICAL PRODUCTS LLC
Labeler DUNS
361287816
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2021-01-27
Public Version
1
Public Version Date
2021-02-04
Public Version Status
New
Public Device Record Key
ec84ef52-0a23-49c8-a6a6-b3566818d4fb

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
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GIO TUBE, COLLECTION, CAPILLARY BLOOD

GMDN Terms

Code Name
61388 Capillary blood collection tube IVD, lithium heparin

Identifiers

Type ID
Unit of Use 15060586450080
Primary 05060586450083

Customer Contacts