FDA UDI In Commercial Distribution 🇺🇸 United States

AOK

DI: 16973869540035 · Model: 20190019 · AOK TOOLING LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
5

Basic Information

Brand Name
AOK
Primary DI
16973869540035
Version / Model
20190019
Company Name
AOK TOOLING LIMITED
Labeler DUNS
544325948
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-11-19
Public Version
1
Public Version Date
2020-11-27
Public Version Status
New
Public Device Record Key
e773f5b6-4914-4601-a13f-2b6f9bd6749d

Device Description

Plan Surgical Face Mask

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FXX Mask, Surgical

GMDN Terms

Code Name
64821 Public face mask, single-use

Identifiers

Type ID
Package 26973869540032
Primary 16973869540035
Package 36973869540039
Unit of Use 06973869540038

Premarket Submissions

Submission Number Supplement Number
K201517 000