FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327055610 · Model: 0620030201 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327055610
Version / Model
0620030201
Catalog Number
620-030-201
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-16
Public Version
1
Public Version Date
2019-12-24
Public Version Status
New
Public Device Record Key
265a38cd-7724-4ba5-af7d-434bea36644e

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
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

Product Codes

Code Name
NKC Tubing/tubing with filter, insufflation, laparoscopic

GMDN Terms

Code Name
38559 Insufflation gas conditioning tubing set

Identifiers

Type ID
Package 37613327055611
Primary 07613327055610

Customer Contacts