FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982240569 · Model: 532.020 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982240569
Version / Model
532.020
Catalog Number
532020
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
4
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
a3357b84-84bc-4f64-9bff-b174361d5396

Device Description

MODIFIED TRINKLE REDUCTION DRIVE UNIT

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
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
GFC DRIVER, SURGICAL, PIN

GMDN Terms

Code Name
64570 Reaming power tool attachment

Identifiers

Type ID
Direct Marking 07611819126992
Secondary H6795320200
Primary 10886982240569

Customer Contacts