FDA UDI In Commercial Distribution 🇺🇸 United States

Stryker F1

DI: 07613327072013 · Model: 1900037000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stryker F1
Primary DI
07613327072013
Version / Model
1900037000
Catalog Number
1900-037-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
2
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
9709fece-3249-4795-90e4-018b56b1c15a

Device Description

Reciprocating Saw

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Hydrogen Peroxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
33541 Bone/joint surgical power tool motor, electric

Identifiers

Type ID
Primary 07613327072013

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius