FDA UDI In Commercial Distribution 🇺🇸 United States

AURELIA REFRESH

DI: 09555002101596 · Model: 99229 · SUPERMAX GLOVE MANUFACTURING SDN. BHD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
AURELIA REFRESH
Primary DI
09555002101596
Version / Model
99229
Company Name
SUPERMAX GLOVE MANUFACTURING SDN. BHD.
Labeler DUNS
652680414
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2024-02-08
Public Version
1
Public Version Date
2024-02-16
Public Version Status
New
Public Device Record Key
6d0b2d35-2ac5-4a46-9366-1bad7592383c

Device Description

Non-sterile Powder Free Latex Examination Gloves

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYY Latex Patient Examination Glove

GMDN Terms

Code Name
47172 Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Unit of Use 19555002101593
Primary 09555002101596

Premarket Submissions

Submission Number Supplement Number
K991415 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius