FDA UDI Not in Commercial Distribution 🇺🇸 United States

FemSoft® Insert Female Urethral Insert

DI: 00801741011115 · Model: 72203 · Rochester Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FemSoft® Insert Female Urethral Insert
Primary DI
00801741011115
Version / Model
72203
Catalog Number
72203
Company Name
Rochester Medical Corporation
Labeler DUNS
605440718
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-03-30
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
dd9d0b00-93c7-468a-8e23-b2d3278f5d24
Distribution End Date
2016-05-12

Device Description

Female Urethral Insert

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
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
OCK Transurethral occlusion insert, urinary incontinence-control, female

GMDN Terms

Code Name
45333 Female-incontinence urethral balloon

Identifiers

Type ID
Package 10801741011112
Primary 00801741011115

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4.5 Centimeter