FDA UDI In Commercial Distribution 🇺🇸 United States

Elite

DI: 00810633021958 · Model: DK-300 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Elite
Primary DI
00810633021958
Version / Model
DK-300
Catalog Number
DK300
Company Name
Synthes GmbH
Labeler DUNS
480426451
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-15
Public Version
7
Public Version Date
2021-11-11
Public Version Status
Update
Public Device Record Key
bbba796c-3ada-48d8-8e2b-0c3ae761ead3

Device Description

BME ELITE INSTRUMENT KIT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 00810633021958

Customer Contacts