FDA UDI In Commercial Distribution 🇺🇸 United States

PANTA®

DI: 10381780052999 · Model: 519130ND · NEWDEAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PANTA®
Primary DI
10381780052999
Version / Model
519130ND
Company Name
NEWDEAL
Labeler DUNS
536935331
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-31
Public Version
7
Public Version Date
2023-02-08
Public Version Status
Update
Public Device Record Key
c1b3a913-05f6-4c52-b93f-0183c842fa63
Distribution End Date
2026-05-26

Device Description

The compression device is part of the system used for the insertion of the nail and to perform compression.

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
46751 Bone holding forceps

Identifiers

Type ID
Secondary M248519130ND1
Primary 10381780052999

Customer Contacts