FDA UDI In Commercial Distribution 🇺🇸 United States

Needle guide TEST

DI: 04547410211214 · Model: NEEDLE GUIDE TEST E · FUJIFILM CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Needle guide TEST
Primary DI
04547410211214
Version / Model
NEEDLE GUIDE TEST E
Company Name
FUJIFILM CORPORATION
Labeler DUNS
713565195
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2023-12-11
Public Version Status
Update
Public Device Record Key
9f65cf8f-3946-474d-9641-102aedb1ea30

Device Description

This guide is used for the Position accuracy check needle.

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MUE Full field digital,system,x-ray,mammographic

GMDN Terms

Code Name
37672 Stationary mammographic x-ray system, digital

Identifiers

Type ID
Primary 04547410211214

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133972 000