FDA UDI Not in Commercial Distribution 🇺🇸 United States

Venture

DI: 00618125114146 · Model: 912022 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5000

Basic Information

Brand Name
Venture
Primary DI
00618125114146
Version / Model
912022
Catalog Number
912022
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5000
Record Status
Published
Publish Date
2022-10-14
Public Version
2
Public Version Date
2023-03-06
Public Version Status
Update
Public Device Record Key
dd7710e0-f7fe-4e96-b42b-f5b44ee86328
Distribution End Date
2023-03-05

Device Description

Nonwoven Sponges, Closed Weave, 4 Ply, 2" x 2"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
44971 General-purpose surgical sponge

Identifiers

Type ID
Unit of Use 80618125114142
Primary 00618125114146