FDA UDI Not in Commercial Distribution 🇺🇸 United States

CLARITY ® RETRACTOR SYSTEM

DI: 00846468044237 · Model: 53-3BL-DILATOR · 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
00846468044237
Version / Model
53-3BL-DILATOR
Company Name
Pioneer Surgical Technology, Inc.
Labeler DUNS
793384496
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-16
Public Version
4
Public Version Date
2021-10-14
Public Version Status
Update
Public Device Record Key
5f0a613c-afeb-4da2-936f-0c1049a526e5
Distribution End Date
2018-06-22

Device Description

3 BLADE RETRACTOR, DILATOR

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00846468044237