FDA UDI In Commercial Distribution 🇺🇸 United States

Mammotome revolve

DI: 00841911102762 · Model: MHUS10 · DEVICOR MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mammotome revolve
Primary DI
00841911102762
Version / Model
MHUS10
Catalog Number
CA000400004
Company Name
DEVICOR MEDICAL PRODUCTS, INC.
Labeler DUNS
961832156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-07
Public Version
1
Public Version Date
2024-10-15
Public Version Status
New
Public Device Record Key
8aa39a45-2e9e-4619-b238-362a25e4aab9

Device Description

Ultrasound Probe - Non-Glass Falcon - CE

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
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
No
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 10841911102769
Primary 00841911102762

Premarket Submissions

Submission Number Supplement Number
K152989 000

Device Sizes

Type Value Unit Text
Needle Gauge 10 Gauge