FDA UDI In Commercial Distribution 🇺🇸 United States

guiding sleeve

DI: 04250337105237 · Model: GTC224353 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
guiding sleeve
Primary DI
04250337105237
Version / Model
GTC224353
Catalog Number
GTC224353
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
0dd90b6b-411d-45b4-8efc-258d66967d06

Device Description

Guiding Tube, conical, yellow

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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
37142 Endoscopic-access dilator, reusable

Identifiers

Type ID
Primary 04250337105237

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify L 223 mm / ID 4.2 mm / OD 5.2 mm