FDA UDI In Commercial Distribution 🇺🇸 United States

NexPak

DI: 00858439001613 · Model: 9110524 · HEMOSTASIS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NexPak
Primary DI
00858439001613
Version / Model
9110524
Company Name
HEMOSTASIS, LLC
Labeler DUNS
801380697
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-30
Public Version
2
Public Version Date
2020-12-21
Public Version Status
Update
Public Device Record Key
262ca99e-eba3-4f51-b0b9-488d4318c01b

Device Description

NexPak Intranasal Splint is a sterile flexible foam pad comprised of a lyophilized mixture of starch polysaccharide and polysaccharide binders. NexPak Intranasal Splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and nasal cavity. The intranasal splint is placed in the nasal cavity after surgery or trauma.

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LYA Splint, Intranasal Septal

GMDN Terms

Code Name
31919 Intranasal splint, non-biodegradable

Identifiers

Type ID
Package 00858439001620
Primary 00858439001613

Customer Contacts

Device Sizes

Type Value Unit Text
Width 0.5 Inch
Length 1.75 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature