FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327057652 · Model: 0377030200 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327057652
Version / Model
0377030200
Catalog Number
0377-030-200
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-26
Public Version
1
Public Version Date
2019-09-03
Public Version Status
New
Public Device Record Key
0c11b8c6-4639-4823-89a8-69f74765019b

Device Description

High-flow Sheath, Single 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
NBH Accessories, arthroscopic

GMDN Terms

Code Name
62458 Arthroscopic access cannula, reusable

Identifiers

Type ID
Primary 07613327057652

Customer Contacts