FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982350121 · Model: SD333.050 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982350121
Version / Model
SD333.050
Catalog Number
SD333050
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-16
Public Version
1
Public Version Date
2025-07-24
Public Version Status
New
Public Device Record Key
7b00c0b4-08bb-4871-b411-d32e8ffb836d

Device Description

FEMORAL GONIOMETER

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
HWT TEMPLATE

GMDN Terms

Code Name
33651 Manual goniometer

Identifiers

Type ID
Primary 10886982350121

Customer Contacts