FDA UDI In Commercial Distribution 🇺🇸 United States

Bending Heaver

DI: 09120047301890 · Model: KJ.207.14 · I.T.S. GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bending Heaver
Primary DI
09120047301890
Version / Model
KJ.207.14
Catalog Number
KJ.207.14
Company Name
I.T.S. GmbH
Labeler DUNS
303456917
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-14
Public Version
1
Public Version Date
2018-12-17
Public Version Status
New
Public Device Record Key
b11c7056-b1d8-42cc-ab42-2faa6104ec15

Device Description

Bending Heaver, 14cm, 3.5mm, 2.7mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
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
HXP Instrument, Bending Or Contouring

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary 09120047301890