FDA UDI In Commercial Distribution 🇺🇸 United States

RULTRACT

DI: B1524160S020 · Model: 4160S-02 · PEMCO INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
RULTRACT
Primary DI
B1524160S020
Version / Model
4160S-02
Catalog Number
4160S-02
Company Name
PEMCO INC
Labeler DUNS
004217071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-21
Public Version
1
Public Version Date
2025-12-01
Public Version Status
New
Public Device Record Key
edf5d488-5b02-4731-b991-fbc9bef22180

Device Description

Spline Tip, Circulator Applied, Post/Clamp

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
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
DWS Instruments, Surgical, Cardiovascular

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary B1524160S020

Customer Contacts

Phone
888-550-5695