FDA UDI In Commercial Distribution 🇺🇸 United States

SUPMEDIC

DI: 00810160180425 · Model: SKF 4304 · Supmedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
SUPMEDIC
Primary DI
00810160180425
Version / Model
SKF 4304
Company Name
Supmedics Inc.
Labeler DUNS
107150886
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-02-12
Public Version
1
Public Version Date
2025-02-20
Public Version Status
New
Public Device Record Key
ac952bac-7126-47fc-a5f7-545e516caeda

Device Description

Powder Free Nitrile Examination Gloves (L size)

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
No
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
Package 00810160180463
Primary 00810160180425
Unit of Use 00810160182016

Premarket Submissions

Submission Number Supplement Number
K213040 000

Device Sizes

Type Value Unit Text
Width 110 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius