FDA UDI In Commercial Distribution 🇺🇸 United States

Omni Hysteroscopy Light Set

DI: 25420045510347 · Model: 60-250-2 · Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Omni Hysteroscopy Light Set
Primary DI
25420045510347
Version / Model
60-250-2
Catalog Number
60-250-2
Company Name
Hologic, Inc.
Labeler DUNS
018925968
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-26
Public Version
1
Public Version Date
2024-10-04
Public Version Status
New
Public Device Record Key
64ef2ba9-d9e4-49d1-b950-973a30ab4205

Device Description

The OMNI™Hysteroscope is used to provide viewing of the cervical canal and the uterine cavity for the purpose of performing diagnostic and surgical procedures.

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HIH Hysteroscope (And Accessories)

GMDN Terms

Code Name
36628 Rigid optical hysteroscope

Identifiers

Type ID
Primary 25420045510347

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182006 000