FDA UDI In Commercial Distribution 🇺🇸 United States

A Plus

DI: 00683534840450 · Model: 1 · A PLUS INTERNATIONAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
A Plus
Primary DI
00683534840450
Version / Model
1
Catalog Number
21-1836-2
Company Name
A PLUS INTERNATIONAL INC.
Labeler DUNS
191705904
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-19
Public Version
1
Public Version Date
2022-10-27
Public Version Status
New
Public Device Record Key
890e734a-74d6-41ec-90dc-6b4c7d497f4f

Device Description

18"X36", Prewashed, Rigid Pack, Bleached White, 3 Pc(s)/Pack, 60 Pc(s)/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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "Moist Heat or Steam Sterilization", "Radiation Sterilization"]

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Package 70683534840459
Primary 00683534840450
Package 80683534840456