FDA UDI In Commercial Distribution 🇺🇸 United States

Spatula

DI: 04946329389845 · Model: 07-959-02 · MIZUHO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spatula
Primary DI
04946329389845
Version / Model
07-959-02
Catalog Number
07-959-02
Company Name
MIZUHO CORPORATION
Labeler DUNS
690677802
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-20
Public Version
1
Public Version Date
2023-03-28
Public Version Status
New
Public Device Record Key
a51d0d2d-4762-4bcb-82ca-a8c5d307618b

Device Description

Spatula 4 mm Stainless

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HAO Instrument, Surgical, Non-Powered

GMDN Terms

Code Name
62772 Neurosurgical retraction system, brain

Identifiers

Type ID
Primary 04946329389845

Customer Contacts

Phone
9999999999

Device Sizes

Type Value Unit Text
Length 200 Millimeter