FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613153092841 · Model: 4125147090S3 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613153092841
Version / Model
4125147090S3
Catalog Number
4125-147-090S3
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-23
Public Version
3
Public Version Date
2022-04-18
Public Version Status
Update
Public Device Record Key
97f8fd39-07a7-4ce7-9693-15e02cccd571

Device Description

Dual Cut Sagittal Blade

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
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
43376 Surgical saw blade, sagittal, single-use

Identifiers

Type ID
Primary 07613153092841

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Cut Edge: 24.5 Millimeter
Depth 100.0 Millimeter
Device Size Text, specify Cut Thickness: 1.5 Millimeter
Device Size Text, specify Material Thickness: 1.38 Millimeter