FDA UDI In Commercial Distribution 🇺🇸 United States

Rejoni Intrauterine Catheter

DI: 00860010540909 · Model: CA-2015-1 · Rejoni, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rejoni Intrauterine Catheter
Primary DI
00860010540909
Version / Model
CA-2015-1
Company Name
Rejoni, Inc.
Labeler DUNS
118420242
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-14
Public Version
1
Public Version Date
2023-07-24
Public Version Status
New
Public Device Record Key
6ef6b365-c2a5-4a28-ac77-c5a7bf20b848

Device Description

The Rejoni Intrauterine Catheter is for the delivery of contrast media or saline into the uterine cavity during Hysterosalpingography (HSG) or Sonohysterography (SHG) for examination of the uterus and fallopian tubes. When used for HSG, the Rejoni Intrauterine Catheter can be used for evaluation of tubal patency. The Rejoni Intrauterine Catheter is used to access the uterine cavity for the delivery of saline for Sonohysterography (SHG).

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
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
LKF Cannula, Manipulator/Injector, Uterine

GMDN Terms

Code Name
18746 Intrauterine imaging medium catheter

Identifiers

Type ID
Primary 00860010540909