FDA UDI In Commercial Distribution 🇺🇸 United States

Trevo XP ProVue Retriever

DI: 00815742000672 · Model: 93067 · Stryker Corporation
Product Codes
0
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trevo XP ProVue Retriever
Primary DI
00815742000672
Version / Model
93067
Catalog Number
93067
Company Name
Stryker Corporation
Labeler DUNS
042405446
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
4
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
bc6ad850-cdb9-482f-a816-92f58325701e

Device Description

Procedure Pack

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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

GMDN Terms

Code Name
10688 Angiographic catheter, single-use
58173 Thrombectomy suction catheter

Identifiers

Type ID
Primary 00815742000672

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dry, dark place.