FDA UDI In Commercial Distribution 🇺🇸 United States

n/a

DI: 07613327467239 · Model: 6000-805-021 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n/a
Primary DI
07613327467239
Version / Model
6000-805-021
Catalog Number
6000-805-021
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-17
Public Version
1
Public Version Date
2023-03-27
Public Version Status
New
Public Device Record Key
ff389eb4-301d-417b-ab16-418d76ae1777

Device Description

Needle Sleeve

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
MR Unsafe
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

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
61496 Surgical planning/navigation-enhancement system

Identifiers

Type ID
Primary 07613327467239

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
10 – 35 Degrees Celsius
Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-20 – 50 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal