FDA UDI In Commercial Distribution 🇺🇸 United States

AURELIA PROTEGE

DI: 09555002102333 · Model: 93998 · SUPERMAX GLOVE MANUFACTURING SDN. BHD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
AURELIA PROTEGE
Primary DI
09555002102333
Version / Model
93998
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
cf7fd080-a233-476f-a30f-c4763163231d

Device Description

Non-sterile Powder Free Nitrile 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
No
Not Made with NRL
Yes
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
LZA Polymer Patient Examination Glove

GMDN Terms

Code Name
56286 Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Unit of Use 19555002102330
Primary 09555002102333

Premarket Submissions

Submission Number Supplement Number
K993258 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius