FDA UDI In Commercial Distribution 🇺🇸 United States

Turtlebrace

DI: 20628634832145 · Model: Wrist Pediatric · 9321-8758 Québec Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Turtlebrace
Primary DI
20628634832145
Version / Model
Wrist Pediatric
Catalog Number
HBPP-02,HBPP-03
Company Name
9321-8758 Québec Inc
Labeler DUNS
203875315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-16
Public Version
1
Public Version Date
2023-01-24
Public Version Status
New
Public Device Record Key
c4027c57-d97f-4d74-87e0-f5623797dbe8

Device Description

The brace is composed of a low-temperature thermoplastic fused between a layer of 3D stretchable knitted fabric and a layer of 3D stretchable knitted velcro receptive fabric. The brace can be molded directly to the patient to immobilize a wrist, with the ability to be remolded to follow the patient's change in morphology (loss of swelling), evolution in a treatment (tendon stretching), correction of deformities, or other reason in accordance with the treatment procedure for a specific patient. This is a multiple use single patient brace. Velcro closure separate. Size medium (02), or large (03), Pediatric (PED)

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
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IQI Orthosis, Limb Brace

GMDN Terms

Code Name
66055 Custom-made upper-limb orthosis

Identifiers

Type ID
Primary 20628634832145

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify PED M for Pediatric Medium
Device Size Text, specify PED L for Pediatric Large