FDA UDI In Commercial Distribution 🇺🇸 United States

RG

DI: G001RG31 · Model: RG3 · Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
RG
Primary DI
G001RG31
Version / Model
RG3
Company Name
Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.
Labeler DUNS
529534554
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-27
Public Version
1
Public Version Date
2025-07-07
Public Version Status
New
Public Device Record Key
6186496b-b209-4223-bf68-54995c6d4198

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MRZ Accessories, Pump, Infusion

GMDN Terms

Code Name
63095 General-purpose syringe/needle

Identifiers

Type ID
Primary G001RG31

Premarket Submissions

Submission Number Supplement Number
K201634 000