FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327058659 · Model: 0250080619 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327058659
Version / Model
0250080619
Catalog Number
0250080619
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
08104725-d556-48e0-a35d-6ff4e74491af

Device Description

Replacement Flush Port Caps

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
No
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
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
OCZ Endoscopic grasping/cutting instrument, non-powered

GMDN Terms

Code Name
37148 Laparoscopic access cannula, reusable

Identifiers

Type ID
Package 37613327058650
Primary 07613327058659

Customer Contacts