FDA UDI In Commercial Distribution 🇺🇸 United States

Snow Lotus

DI: 06936610210109 · Model: M · Beijing Reagent Latex Products Factory
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Snow Lotus
Primary DI
06936610210109
Version / Model
M
Company Name
Beijing Reagent Latex Products Factory
Labeler DUNS
653865840
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2021-09-18
Public Version
1
Public Version Date
2021-09-27
Public Version Status
New
Public Device Record Key
bf7f9f27-e214-4db2-9ed1-b246fb9998a3

Device Description

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
Yes
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
Package 16936610210106
Primary 06936610210109
Unit of Use 26936610210103

Premarket Submissions

Submission Number Supplement Number
K010947 000