FDA UDI In Commercial Distribution 🇺🇸 United States

PRO

DI: 07613327131833 · Model: 705450 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRO
Primary DI
07613327131833
Version / Model
705450
Catalog Number
705450
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2021-06-23
Public Version Status
Update
Public Device Record Key
688a2631-16ab-48e9-b342-443d71e7c5b2

Device Description

Jaw Clamp

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
HXD CLAMP

GMDN Terms

Code Name
34949 Bone approximation clamp

Identifiers

Type ID
Primary 07613327131833