FDA UDI In Commercial Distribution 🇺🇸 United States

Summit Doppler

DI: 00888937010053 · Model: C250CP · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Summit Doppler
Primary DI
00888937010053
Version / Model
C250CP
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-21
Public Version
5
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
90d589e9-8437-4a17-a9a0-721e70340299

Device Description

LifeDop 250 Professional with 2.0 MHz, 3.0 MHz and 5.0 MHz EchoHeart Transvaginal Probes

Device Characteristics

Single Use
No
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
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
KNG Monitor, Ultrasonic, Fetal

GMDN Terms

Code Name
34040 Foetal Doppler system

Identifiers

Type ID
Package 60888937010055
Primary 00888937010053

Premarket Submissions

Submission Number Supplement Number
K024197 000