FDA UDI In Commercial Distribution 🇺🇸 United States

dissector

DI: 04250337111672 · Model: JDA243515 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
dissector
Primary DI
04250337111672
Version / Model
JDA243515
Catalog Number
JDA243515
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
576c3858-08f7-4616-a521-b96e74ed3e32

Device Description

Dissector

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
Yes
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
FZS CURETTE, SURGICAL, GENERAL USE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 04250337111672

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify WL 240 mm / OD 3.5 mm