FDA UDI In Commercial Distribution 🇺🇸 United States

Slide stopper TEST

DI: 04547410211207 · Model: LATERAL NEEDLE STOPPER TEST E · FUJIFILM CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Slide stopper TEST
Primary DI
04547410211207
Version / Model
LATERAL NEEDLE STOPPER 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
ce0e088e-a922-454d-bab5-8beb10b8c9d5

Device Description

Adjust the depth that the needle is inserted. The slide stopper differs for each needle. Use a slide stopper that suits each type of needle being used.

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 04547410211207

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133972 000