FDA UDI In Commercial Distribution 🇺🇸 United States

AmbiCanner

DI: 00854947005907 · Model: 470-7-AM · SUMMIT GLOVE INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
24

Basic Information

Brand Name
AmbiCanner
Primary DI
00854947005907
Version / Model
470-7-AM
Company Name
SUMMIT GLOVE INC.
Labeler DUNS
054386458
Distribution Status
In Commercial Distribution
Device Count in Pkg
24
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
4f863c02-526b-4b62-8ada-6535b8ee9165

Device Description

12mil, 12" in length, Latex, Examination Grade, Unlined, Ambidextrous, Fishscale, Beaded Cuff, Amber Color, Size Small

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
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
Package 10854947005904
Primary 00854947005907
Unit of Use 00854947005914

Customer Contacts

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