FDA UDI In Commercial Distribution 🇺🇸 United States

Saneck Safety

DI: 00705689014712 · Model: SEPF-4.3-WH-MD · The Cannon Group, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Saneck Safety
Primary DI
00705689014712
Version / Model
SEPF-4.3-WH-MD
Company Name
The Cannon Group, Inc.
Labeler DUNS
131884975
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-02-06
Public Version
1
Public Version Date
2025-02-14
Public Version Status
New
Public Device Record Key
e0849f7f-d81e-4f1a-ab48-c6ce147f965a

Device Description

MEDIUM SYNTHETIC VINYL 4.3MIL PF EXAM GLOVE 10/100

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYZ Vinyl Patient Examination Glove

GMDN Terms

Code Name
47176 Vinyl examination/treatment glove, non-powdered

Identifiers

Type ID
Package 00705689014729
Primary 00705689014712
Unit of Use 10705689014719