FDA UDI In Commercial Distribution 🇺🇸 United States

AdvanceFit

DI: 00850019992229 · Model: 650-OR-M · SUMMIT GLOVE INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
4

Basic Information

Brand Name
AdvanceFit
Primary DI
00850019992229
Version / Model
650-OR-M
Company Name
SUMMIT GLOVE INC.
Labeler DUNS
054386458
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2020-08-01
Public Version
1
Public Version Date
2020-08-10
Public Version Status
New
Public Device Record Key
4908f071-68f0-481b-bd01-d390f6bcd4d0

Device Description

4.5mil, 9.5" in Length, Nitrile, Examination Grade, Ambidextrous, Powder Free, Beaded Cuff, Orange Color, Size Medium Sample Pack

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Package 10850019992226
Primary 00850019992229
Unit of Use 00850019992236

Customer Contacts

Phone
+1(330)868-0066 ext. 15