FDA UDI In Commercial Distribution 🇺🇸 United States

joimax®

DI: 04250337100041 · Model: AS4070175 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
joimax®
Primary DI
04250337100041
Version / Model
AS4070175
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
4260cd60-f36d-4baa-81f5-feb11fe1e377

Device Description

joimax® Arthroscope Combo WL 175 mm / OD 4.0 mm / 70°

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
HRX Arthroscope

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 04250337100041

Customer Contacts

Phone
+49721255140

Premarket Submissions

Submission Number Supplement Number
K051827 000