FDA UDI In Commercial Distribution 🇺🇸 United States

Mammotome

DI: 00841911101888 · Model: MRLB1 · DEVICOR MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mammotome
Primary DI
00841911101888
Version / Model
MRLB1
Company Name
DEVICOR MEDICAL PRODUCTS, INC.
Labeler DUNS
961832156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-08
Public Version
1
Public Version Date
2022-02-16
Public Version Status
New
Public Device Record Key
35d30dd9-cced-413e-9a9b-c95108a3d199

Device Description

Control Module MR Interlock System

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNW Instrument, Biopsy

GMDN Terms

Code Name
36190 Mammographic stereotactic biopsy system

Identifiers

Type ID
Primary 00841911101888

Customer Contacts

Phone
877-926-2666

Premarket Submissions

Submission Number Supplement Number
K042753 000

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-35 – 54 Degrees Celsius