FDA UDI In Commercial Distribution 🇺🇸 United States

Double IUD Extractor

DI: 00888937019667 · Model: 392-151 · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Double IUD Extractor
Primary DI
00888937019667
Version / Model
392-151
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-30
Public Version
3
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
ecb36354-efcc-4fe1-a565-56542adf9fe1

Device Description

Double IUD Extractor

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
HHF Remover, Intrauterine Device, Contraceptive, Hook-Type

GMDN Terms

Code Name
12032 Intrauterine device removal hook, reusable

Identifiers

Type ID
Primary 00888937019667

Device Sizes

Type Value Unit Text
Length 262 Millimeter