FDA UDI Not in Commercial Distribution 🇺🇸 United States

SOMATEX

DI: 08033860021634 · Model: SOMACORE VERIFY · BIOPSYBELL SRL
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
SOMATEX
Primary DI
08033860021634
Version / Model
SOMACORE VERIFY
Catalog Number
900390-US
Company Name
BIOPSYBELL SRL
Labeler DUNS
438746708
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
6
Public Version Date
2025-04-29
Public Version Status
Update
Public Device Record Key
278e57e0-7a09-4f12-9b2e-93ae37b609f7
Distribution End Date
2025-04-28

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNW Instrument, Biopsy
FCG Biopsy Needle

GMDN Terms

Code Name
16835 Soft-tissue biopsy procedure kit, non-medicated

Identifiers

Type ID
Package 08033860021641
Primary 08033860021634

Customer Contacts

Phone
+39053527850

Premarket Submissions

Submission Number Supplement Number
K130616 000

Device Sizes

Type Value Unit Text
Length 100 Millimeter
Needle Gauge 16 Gauge