FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Gauze Sponge

DI: 00616784322223 · Model: 3222 · Dynarex Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Surgical Gauze Sponge
Primary DI
00616784322223
Version / Model
3222
Company Name
Dynarex Corporation
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2021-06-21
Public Version
3
Public Version Date
2026-03-11
Public Version Status
Update
Public Device Record Key
73ccf827-36f9-4d22-9b2a-d01d5640178b

Device Description

Surgical Gauze Sponge, All Gauze, 2"x2", 8 ply

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
Yes
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
Package 00616784322230
Primary 00616784322223
Unit of Use 00810180844116