FDA UDI In Commercial Distribution 🇺🇸 United States

Akers

DI: 00759326084033 · Model: g803 · Akers Industries, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Akers
Primary DI
00759326084033
Version / Model
g803
Company Name
Akers Industries, Inc.
Labeler DUNS
790695126
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2022-11-09
Public Version
1
Public Version Date
2022-11-17
Public Version Status
New
Public Device Record Key
ced5abf2-4242-4230-991e-9b8af1c08a8b

Device Description

late powder free latex examination gloves

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
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 00759326684134
Primary 00759326084033

Premarket Submissions

Submission Number Supplement Number
K993567 000