FDA UDI In Commercial Distribution 🇺🇸 United States

Saniflex

DI: 16973163407119 · Model: KF-B P05(L3) · Guangdong KINGFA SCI.&TECH. Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Saniflex
Primary DI
16973163407119
Version / Model
KF-B P05(L3)
Company Name
Guangdong KINGFA SCI.&TECH. Co., Ltd.
Labeler DUNS
543265548
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2021-10-12
Public Version
1
Public Version Date
2021-10-20
Public Version Status
New
Public Device Record Key
79708aff-e67c-47b6-90fc-ed552996b477

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
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
FXX Mask, Surgical

GMDN Terms

Code Name
35177 Surgical/medical face mask, single-use

Identifiers

Type ID
Package 26973163407116
Primary 16973163407119
Unit of Use 06973163407112

Premarket Submissions

Submission Number Supplement Number
K202139 000