FDA UDI In Commercial Distribution 🇺🇸 United States

OTIS

DI: 03760154001083 · Model: Impactor body · S.B.M
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OTIS
Primary DI
03760154001083
Version / Model
Impactor body
Catalog Number
EVO9069444
Company Name
S.B.M
Labeler DUNS
772462123
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-19
Public Version
1
Public Version Date
2023-12-27
Public Version Status
New
Public Device Record Key
a16db903-88f7-4f08-9ed6-e04a7dc0b02c

Device Description

Impactor body to be used with OTIS implants for HTO.

Device Characteristics

Single Use
Yes
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
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
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 03760154001083