FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613154248377 · Model: 52-27214E · Stryker GmbH
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
07613154248377
Version / Model
52-27214E
Catalog Number
52-27214E
Company Name
Stryker GmbH
Labeler DUNS
481999654
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-23
Public Version
6
Public Version Date
2025-04-14
Public Version Status
Update
Public Device Record Key
0dbd355f-177d-4e40-bd1f-3f8fa6d482bf
Distribution End Date
2022-07-29

Device Description

BONE SCREW, CROSS-PIN, SELF-TAPPING

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 07613154248377

Device Sizes

Type Value Unit Text
Length 14.0 Millimeter
Device Size Text, specify Diameter: 2.7 Millimeter