FDA UDI In Commercial Distribution 🇺🇸 United States

CarePak

DI: 00017276229158 · Model: 017276229158 · Aso LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
15

Basic Information

Brand Name
CarePak
Primary DI
00017276229158
Version / Model
017276229158
Company Name
Aso LLC
Labeler DUNS
152793493
Distribution Status
In Commercial Distribution
Device Count in Pkg
15
Record Status
Published
Publish Date
2020-07-29
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
32dc283a-52e4-4e2d-a18d-9d17d954e0a8

Device Description

Sterile Pads, all one size, 2 IN x 2 IN (50 mm x 50 mm)

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
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Package 10017276229155
Primary 00017276229158
Unit of Use 60017276229150

Customer Contacts