FDA UDI In Commercial Distribution 🇺🇸 United States

OTIS-F

DI: 03760154008174 · Model: OTIS-F AO drill guide · S.B.M
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OTIS-F
Primary DI
03760154008174
Version / Model
OTIS-F AO drill guide
Catalog Number
EVO90T4000
Company Name
S.B.M
Labeler DUNS
772462123
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-20
Public Version
1
Public Version Date
2024-06-28
Public Version Status
New
Public Device Record Key
1af2ea3a-42bc-444e-b7b8-70d511404d78

Device Description

AO drill guide

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
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
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 03760154008174