FDA UDI In Commercial Distribution 🇺🇸 United States

RULTRACT

DI: B1524150S010 · Model: 4150S-01 · PEMCO INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RULTRACT
Primary DI
B1524150S010
Version / Model
4150S-01
Catalog Number
4150S-01
Company Name
PEMCO INC
Labeler DUNS
004217071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-11
Public Version
1
Public Version Date
2024-03-19
Public Version Status
New
Public Device Record Key
829e34e7-9340-4ed3-bbb8-5f633a4943f8

Device Description

Spline Tip, Post/Clamp, Scrub Applied

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
Yes
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
DWS Instruments, Surgical, Cardiovascular

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary B1524150S010

Customer Contacts

Phone
888-550-5695