FDA UDI In Commercial Distribution 🇺🇸 United States

Lead Hand Pediatric

DI: 00192896109230 · Model: 48-0339 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lead Hand Pediatric
Primary DI
00192896109230
Version / Model
48-0339
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-06
Public Version
1
Public Version Date
2021-05-14
Public Version Status
New
Public Device Record Key
d9df0739-7353-486c-82d6-8081ab365806

Device Description

Lead Hand Pediatric

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
FMQ Restraint, protective

GMDN Terms

Code Name
62482 Limb/torso/head restraint, reusable

Identifiers

Type ID
Primary 00192896109230

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9.75 Inch