FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00850231007329 · Model: II-1-0005 · Integrity Implants Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00850231007329
Version / Model
II-1-0005
Catalog Number
II-1-0005
Company Name
Integrity Implants Inc.
Labeler DUNS
080300717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-22
Public Version
4
Public Version Date
2022-05-13
Public Version Status
Update
Public Device Record Key
056660dc-1ed0-4755-916a-8d14c8b962fe

Device Description

Slap Hammer

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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
47814 Orthopaedic implantation hammering attachment

Identifiers

Type ID
Primary 00850231007329

Customer Contacts

Phone
8002019300