FDA UDI In Commercial Distribution 🇺🇸 United States

LEEP Endocervical Speculum

DI: 00888937016253 · Model: F510 · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LEEP Endocervical Speculum
Primary DI
00888937016253
Version / Model
F510
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-16
Public Version
4
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
a3823c09-1beb-4d26-bbcf-6878e8c99621

Device Description

LEEP Endocervical Speculum - Coated- Medium

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
Yes
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
HFB Forceps, Biopsy, Gynecological

GMDN Terms

Code Name
16469 Manual expandable cervical dilator

Identifiers

Type ID
Primary 00888937016253

Device Sizes

Type Value Unit Text
Width 5 Millimeter
Length 273 Millimeter