FDA UDI Not in Commercial Distribution 🇺🇸 United States

AUTO LOCK TOURNIQUET

DI: 00192896090682 · Model: 1100-782 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AUTO LOCK TOURNIQUET
Primary DI
00192896090682
Version / Model
1100-782
Catalog Number
1100-782
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
4
Public Version Date
2023-07-26
Public Version Status
Update
Public Device Record Key
acd4bde5-463b-42b5-a830-487f329672a1
Distribution End Date
2023-07-25

Device Description

AUTO LOCK TOURNIQUET

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
MWH pulmonic valved conduit

GMDN Terms

Code Name
35844 Limb tourniquet, manual, reusable

Identifiers

Type ID
Primary 00192896090682

Customer Contacts