FDA UDI In Commercial Distribution 🇺🇸 United States

Hallu®- LOCK

DI: 10381780052012 · Model: 299070ND · NEWDEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Hallu®- LOCK
Primary DI
10381780052012
Version / Model
299070ND
Company Name
NEWDEAL
Labeler DUNS
536935331
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-26
Public Version
3
Public Version Date
2023-02-06
Public Version Status
Update
Public Device Record Key
84e6ef37-cf54-481e-a9a8-b58c6d5c8bc6
Distribution End Date
2027-05-26

Device Description

The left plate bender is used to bend the Hallu® Lock C plate in combination with the right plate bender in order to match the degree of dorsal flexion required by the case or by the activity of the patient.

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
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
HXW BENDER

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Secondary M248299070ND1
Primary 10381780052012

Customer Contacts