FDA UDI In Commercial Distribution 🇺🇸 United States

Sinrel

DI: 06978146200001 · Model: YF1503 · SHENZHEN SINREL TECH LTD
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Sinrel
Primary DI
06978146200001
Version / Model
YF1503
Company Name
SHENZHEN SINREL TECH LTD
Labeler DUNS
618769254
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-09
Public Version
1
Public Version Date
2025-01-17
Public Version Status
New
Public Device Record Key
33852ad1-c146-4415-b941-4a3d15ba1911

Device Description

TENS & PMS Unit

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Package 16978146200008
Primary 06978146200001
Package 26978146200005
Package 36978146200002

Premarket Submissions

Submission Number Supplement Number
K220005 000