FDA UDI In Commercial Distribution 🇺🇸 United States

CLARITY RETRACTOR SYSTEM

DI: 00846468086671 · Model: 51-GUIDEWIRE · Pioneer Surgical Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CLARITY RETRACTOR SYSTEM
Primary DI
00846468086671
Version / Model
51-GUIDEWIRE
Catalog Number
51-GUIDEWIRE
Company Name
Pioneer Surgical Technology, Inc.
Labeler DUNS
793384496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-25
Public Version
2
Public Version Date
2021-10-14
Public Version Status
Update
Public Device Record Key
e8107019-c4dc-40ac-b21c-4756b5243af8

Device Description

MIS GUIDEWIRE, QTY 1

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
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
HXI PASSER, WIRE, ORTHOPEDIC

GMDN Terms

Code Name
61467 General external orthopaedic fixation system implantation kit, single-use

Identifiers

Type ID
Primary 00846468086671

Customer Contacts