FDA UDI In Commercial Distribution 🇺🇸 United States

MyoSure Tissue Removal System Control Unit

DI: 15420045505124 · Model: 10-550 · Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyoSure Tissue Removal System Control Unit
Primary DI
15420045505124
Version / Model
10-550
Catalog Number
10-550
Company Name
Hologic, Inc.
Labeler DUNS
018925968
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-19
Public Version
4
Public Version Date
2023-08-07
Public Version Status
Update
Public Device Record Key
10443041-f914-4cce-a97a-578efb08de6b

Device Description

The MyoSure®Tissue Removal System is intended for hysteroscopic intrauterine resection procedures by a trained gynecologist to hysteroscopically resect and remove tissue such as submucous myomas, endometrial polyps, and retained products of conception.

Device Characteristics

Single Use
No
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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HIH HYSTEROSCOPE (AND ACCESSORIES)

GMDN Terms

Code Name
46729 Tissue morcellation system

Identifiers

Type ID
Primary 15420045505124

Premarket Submissions

Submission Number Supplement Number
K152723 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
High: 93 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-15 – 40 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
381 – 787 Millimeter of Mercury