FDA UDI In Commercial Distribution 🇺🇸 United States

PRO-SPEC

DI: 00810112599732 · Model: TRIAL INSERTER FOR PRO-SPEC SYSTEM · CROSSROADS EXTREMITY SYSTEMS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PRO-SPEC
Primary DI
00810112599732
Version / Model
TRIAL INSERTER FOR PRO-SPEC SYSTEM
Catalog Number
03.845.999
Company Name
CROSSROADS EXTREMITY SYSTEMS
Labeler DUNS
058864308
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-13
Public Version
1
Public Version Date
2025-03-21
Public Version Status
New
Public Device Record Key
cba6c644-4c59-4045-b21e-0c73f9bf9245

Device Description

TRIAL INSERTER FOR PRO-SPEC SYSTEM

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
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Primary 00810112599732