FDA UDI In Commercial Distribution 🇺🇸 United States

Mammotome revolve

DI: 00841911100652 · Model: MCART1 · DEVICOR MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mammotome revolve
Primary DI
00841911100652
Version / Model
MCART1
Company Name
DEVICOR MEDICAL PRODUCTS, INC.
Labeler DUNS
961832156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
328bca7f-2d96-41a6-b7a9-d1ed590a0a29

Device Description

Cart

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
KNW Instrument, Biopsy

GMDN Terms

Code Name
36190 Mammographic stereotactic biopsy system

Identifiers

Type ID
Primary 00841911100652

Customer Contacts

Phone
877-926-2666

Premarket Submissions

Submission Number Supplement Number
K152989 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-18 – 54 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal