FDA UDI In Commercial Distribution 🇺🇸 United States

Kitazato OPU Needle Type2-v6

DI: 04580303269145 · Model: 351304 Type2-v6 · KITAZATO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kitazato OPU Needle Type2-v6
Primary DI
04580303269145
Version / Model
351304 Type2-v6
Catalog Number
351304
Company Name
KITAZATO CORPORATION
Labeler DUNS
711091157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-09
Public Version
8
Public Version Date
2023-08-07
Public Version Status
Update
Public Device Record Key
920c1405-e032-48a8-bc9d-a63a8b289a17

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
Yes
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
MQE NEEDLE, ASSISTED REPRODUCTION

GMDN Terms

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

Identifiers

Type ID
Package 14580303269142
Primary 04580303269145

Premarket Submissions

Submission Number Supplement Number
K112462 000