FDA UDI In Commercial Distribution 🇺🇸 United States

Kleiner KG2 system

DI: 08720246782929 · Model: Trial, 11x36x15mm Parallel · Baat Medical Products B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kleiner KG2 system
Primary DI
08720246782929
Version / Model
Trial, 11x36x15mm Parallel
Catalog Number
02-50215
Company Name
Baat Medical Products B.V.
Labeler DUNS
413205480
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-14
Public Version
1
Public Version Date
2022-12-22
Public Version Status
New
Public Device Record Key
6fcd84ba-f9c2-42ae-be53-34fb7c08e2ab

Device Description

Trial

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
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 08720246782929