FDA UDI In Commercial Distribution 🇺🇸 United States

ABBI

DI: 60888937014183 · Model: ABBI-KIT · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ABBI
Primary DI
60888937014183
Version / Model
ABBI-KIT
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-06
Public Version
5
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
51691aff-834a-431c-ad97-61b05595f0a0

Device Description

ABBI™ KIT (Air Bubble Based Infuser) For office based Sono HSG Procedures

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
37552 Fallopian tube catheterization kit

Identifiers

Type ID
Primary 60888937014183

Premarket Submissions

Submission Number Supplement Number
K143415 000