FDA UDI In Commercial Distribution 🇺🇸 United States

Inrad

DI: 00817295020824 · Model: 681018 · Inrad
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Inrad
Primary DI
00817295020824
Version / Model
681018
Company Name
Inrad
Labeler DUNS
940023385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-01
Public Version
4
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
ca71a95e-70c5-4191-94b1-4938abdd7e94

Device Description

PreciseCore Biopsy 18 ga x 10 cm 20 mm notch

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 10817295020821
Primary 00817295020824

Customer Contacts

Phone
6163017800

Premarket Submissions

Submission Number Supplement Number
K093399 000