FDA UDI In Commercial Distribution 🇺🇸 United States

DCP

DI: 10886982159014 · Model: 226.20 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DCP
Primary DI
10886982159014
Version / Model
226.20
Catalog Number
22620
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
81f225aa-bd0f-42ac-95d7-0a6e8e49943d

Device Description

4.5MM BROAD DCP PLATE 20 HOLES/326MM

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
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
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H679226200
Primary 10886982159014

Customer Contacts