FDA UDI In Commercial Distribution 🇺🇸 United States

XprESS LoProfile

DI: 00857326005017 · Model: MSB&LLF · STRYKER CORPORATION
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
XprESS LoProfile
Primary DI
00857326005017
Version / Model
MSB&LLF
Catalog Number
LPLF-106
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-27
Public Version
9
Public Version Date
2026-01-12
Public Version Status
Update
Public Device Record Key
aea41d2e-8adc-4737-ba6e-dc11278355ed

Device Description

ENT Dilation System 6x20mm

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
No
PM Exempt
No
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
LRC Instrument, Ent Manual Surgical
PNZ Eustachian Tube Balloon Dilation Device

GMDN Terms

Code Name
10718 Eustachian catheter, single-use
48140 Nasal/paranasal balloon catheter, non-tracking

Identifiers

Type ID
Primary 00857326005017
Package 10857326005014