FDA UDI In Commercial Distribution 🇺🇸 United States

Non-Woven Sponge

DI: 00616784325224 · Model: 3252 · DYNAREX CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
Non-Woven Sponge
Primary DI
00616784325224
Version / Model
3252
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2021-09-01
Public Version
1
Public Version Date
2021-09-09
Public Version Status
New
Public Device Record Key
b15b306b-a7de-4640-a391-ee870dfdc218

Device Description

Non-Woven Sponge, 2"x2", 4-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
MR Safe
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
FRL Fiber, Medical, Absorbent

GMDN Terms

Code Name
48130 Non-woven gauze pad, non-sterile

Identifiers

Type ID
Package 00616784325231
Primary 00616784325224
Unit of Use 00616784325217