FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327643855 · Model: 7900132000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NA
Primary DI
07613327643855
Version / Model
7900132000
Catalog Number
7900-132-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-19
Public Version
1
Public Version Date
2025-12-29
Public Version Status
New
Public Device Record Key
f030ffa1-2844-4d2d-872c-ed9fe47f3074

Device Description

5/32" DRILL W/KEY

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
31048 Surgical drill chuck

Identifiers

Type ID
Primary 07613327643855

Customer Contacts

Storage Conditions

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