FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 37613327122962 · Model: 29-93003 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
NA
Primary DI
37613327122962
Version / Model
29-93003
Catalog Number
29-93003
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2018-04-13
Public Version
5
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
9c72a464-dc9f-4794-a2ee-2e5884349aaf

Device Description

3D MESH SILICON MAT

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
LRP TRAY, SURGICAL

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 37613327122962
Unit of Use 07613327122961