FDA UDI In Commercial Distribution 🇺🇸 United States

Mammotome MammoTest

DI: 00841911101208 · Model: G1621 · DEVICOR MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mammotome MammoTest
Primary DI
00841911101208
Version / Model
G1621
Catalog Number
G1621
Company Name
DEVICOR MEDICAL PRODUCTS, INC.
Labeler DUNS
961832156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-10
Public Version
4
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
f38f88ee-c071-4306-8aa8-c6d317f1ac39

Device Description

Fischer Probe Guide Holder

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYN System, Imaging, Pulsed Doppler, Ultrasonic

GMDN Terms

Code Name
60734 Needle guide, reusable

Identifiers

Type ID
Direct Marking 00841911101758
Primary 00841911101208

Customer Contacts

Phone
877-926-2666

Premarket Submissions

Submission Number Supplement Number
K943863 000