FDA UDI In Commercial Distribution 🇺🇸 United States

Dynarex ActiSplint

DI: 00616784352916 · Model: 3529 · DYNAREX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dynarex ActiSplint
Primary DI
00616784352916
Version / Model
3529
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-01
Public Version
1
Public Version Date
2021-09-09
Public Version Status
New
Public Device Record Key
a804aed8-741b-4c83-8647-b7d85b4d623c

Device Description

Dynarex ActiSplint Flat, 36in. Folded Flat Splint, Breathable, Red/Charcoal Gray

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile

GMDN Terms

Code Name
63273 First aid limb splint, mouldable, reusable

Identifiers

Type ID
Package 00616784352930
Primary 00616784352916