FDA UDI In Commercial Distribution 🇺🇸 United States

UNIVERSAL

DI: 08055002900003 · Model: UN18100-00 · MEDAX SRL UNIPERSONALE
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
UNIVERSAL
Primary DI
08055002900003
Version / Model
UN18100-00
Company Name
MEDAX SRL UNIPERSONALE
Labeler DUNS
440211428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-10
Public Version
3
Public Version Date
2026-04-28
Public Version Status
Update
Public Device Record Key
a84700d8-c95f-49e3-8a2b-246c8f7568a4

Device Description

Biopsy needle 18G x 100 mm

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
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
16835 Soft-tissue biopsy procedure kit, non-medicated

Identifiers

Type ID
Primary 08055002900003
Package 18055002900000

Premarket Submissions

Submission Number Supplement Number
K181803 000