FDA UDI In Commercial Distribution 🇺🇸 United States

Mammotome Revolve EX

DI: 00841911102342 · Model: MHEX08S · DEVICOR MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mammotome Revolve EX
Primary DI
00841911102342
Version / Model
MHEX08S
Catalog Number
CA000460001
Company Name
DEVICOR MEDICAL PRODUCTS, INC.
Labeler DUNS
961832156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-28
Public Version
1
Public Version Date
2025-09-05
Public Version Status
New
Public Device Record Key
b9b5076d-39b2-4192-a4a6-b90ac8dde12d

Device Description

Revolve EX Ultrasound Probe with Sleeve - System Registered- CE

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNW Instrument, Biopsy

GMDN Terms

Code Name
58990 Side-notch biopsy gun handpiece/needle

Identifiers

Type ID
Package 10841911102349
Primary 00841911102342

Premarket Submissions

Submission Number Supplement Number
K202012 000