FDA UDI In Commercial Distribution 🇺🇸 United States

Mammotome revolve MammoMark

DI: 00841911101376 · Model: MMK0801 · DEVICOR MEDICAL PRODUCTS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mammotome revolve MammoMark
Primary DI
00841911101376
Version / Model
MMK0801
Company Name
DEVICOR MEDICAL PRODUCTS, INC.
Labeler DUNS
961832156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-01
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
53413417-995f-4b12-b684-0ef3aaa2650a

Device Description

Biopsy Site Identifier

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NEU Marker, Radiographic, Implantable
FZP Clip, Implantable

GMDN Terms

Code Name
40808 Radiological image marker, implantable

Identifiers

Type ID
Package 10841911101373
Primary 00841911101376

Customer Contacts

Phone
877-926-2666

Premarket Submissions

Submission Number Supplement Number
K082278 000

Device Sizes

Type Value Unit Text
Needle Gauge 8 Gauge