FDA UDI In Commercial Distribution 🇺🇸 United States

n/a

DI: 00822409089970 · Model: 800-0119 · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n/a
Primary DI
00822409089970
Version / Model
800-0119
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-19
Public Version
1
Public Version Date
2020-08-27
Public Version Status
New
Public Device Record Key
5f12dba6-1e84-4db3-8119-4606ceb19d1f

Device Description

Stem Broach sz19

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
36167 Orthopaedic broach

Identifiers

Type ID
Primary 00822409089970

Customer Contacts