FDA UDI Not in Commercial Distribution 🇺🇸 United States

SteriGear

DI: 01618125155346 · Model: 28016 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SteriGear
Primary DI
01618125155346
Version / Model
28016
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
3
Public Version Date
2022-09-23
Public Version Status
Update
Public Device Record Key
d1c35f84-b032-45cf-88f4-c7939b35d6c7
Distribution End Date
2022-09-22

Device Description

SteriGear Band Bags Clear Polyethylene Sterile 36in x 28in x 1in 25 per Case

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
61676 Urological fluid funnel, sterile

Identifiers

Type ID
Primary 01618125155346