FDA UDI In Commercial Distribution 🇺🇸 United States

Blade, Titanium lateral fenestrated width 20mm 35mm

DI: 04057034264393 · Model: UL7189-20-35T · Geister Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Blade, Titanium lateral fenestrated width 20mm 35mm
Primary DI
04057034264393
Version / Model
UL7189-20-35T
Catalog Number
UL7189-20-35T
Company Name
Geister Medizintechnik GmbH
Labeler DUNS
343548848
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-18
Public Version
1
Public Version Date
2018-11-19
Public Version Status
New
Public Device Record Key
5e069918-1385-4826-8a61-2b1ae75ffb90

Device Description

Blade, Titanium lateral fenestrated width 20mm 35mm G BLUE LABEL™

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
No

Product Codes

Code Name
GZT RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY

GMDN Terms

Code Name
35967 Surgical retraction system mounting frame, reusable

Identifiers

Type ID
Primary 04057034264393

Customer Contacts