FDA UDI In Commercial Distribution 🇺🇸 United States

RING RETRACTOR LOCK

DI: 00192896101609 · Model: 516-874 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RING RETRACTOR LOCK
Primary DI
00192896101609
Version / Model
516-874
Catalog Number
516-874
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-11
Public Version
3
Public Version Date
2023-07-21
Public Version Status
Update
Public Device Record Key
5109b46d-b566-4815-a2be-5b3b44507f1b

Device Description

STANDARD RING RETRACTOR LOCK, ACCESSORY

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
Yes
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", "Dry Heat Sterilization"]

Product Codes

Code Name
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary 00192896101609

Customer Contacts