FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613327057669 · Model: 0377030201 · STRYKER CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327057669
Version / Model
0377030201
Catalog Number
0377-030-201
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-26
Public Version
3
Public Version Date
2020-02-03
Public Version Status
Update
Public Device Record Key
cacef4ec-7fc9-4a5b-b817-cb7b44a8d032
Distribution End Date
2020-02-03

Device Description

High-flow Sheath, Dual stopcock

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT
NBH Accessories, arthroscopic

GMDN Terms

Code Name
62458 Arthroscopic access cannula, reusable

Identifiers

Type ID
Primary 07613327057669

Customer Contacts