FDA UDI In Commercial Distribution 🇺🇸 United States

Needle / Guide Wire - Set

DI: 04250337103929 · Model: JMSN18GW11 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Needle / Guide Wire - Set
Primary DI
04250337103929
Version / Model
JMSN18GW11
Catalog Number
JMSN18GW11
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
f811eb5b-b0f0-45f4-b199-b89a87ba2fa6

Device Description

joimax® Needle and Guide Wire Set

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAA NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

GMDN Terms

Code Name
37890 Lumbar decompression procedure kit

Identifiers

Type ID
Package 04250337103936
Primary 04250337103929

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 18G Needle L 110 mm, Guide Wire 300 mm