FDA UDI Not in Commercial Distribution 🇺🇸 United States

Venture

DI: 00618125107926 · Model: 260002 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
8000

Basic Information

Brand Name
Venture
Primary DI
00618125107926
Version / Model
260002
Catalog Number
260002
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
8000
Record Status
Published
Publish Date
2022-10-14
Public Version
2
Public Version Date
2023-02-28
Public Version Status
Update
Public Device Record Key
f663fa28-1ea4-4e20-8a60-e799034da81d
Distribution End Date
2023-02-27

Device Description

Nonwoven Sponges, Open 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 80618125107922
Primary 00618125107926