FDA UDI In Commercial Distribution 🇺🇸 United States

SCHWERT

DI: E896169710007E0 · Model: 1697-100-07E · A. Schweickhardt GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCHWERT
Primary DI
E896169710007E0
Version / Model
1697-100-07E
Catalog Number
1697-100-07E
Company Name
A. Schweickhardt GmbH & Co. KG
Labeler DUNS
341195628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-07
Public Version
1
Public Version Date
2025-04-15
Public Version Status
New
Public Device Record Key
b0a80331-49cc-401c-a02b-e7daf4310d06

Device Description

Bone Augmentation Set with SCHWERT Ergo design handle Orange

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
EKR PLUGGER, ROOT CANAL, ENDODONTIC

GMDN Terms

Code Name
38168 Periosteal elevator, reusable

Identifiers

Type ID
Primary E896169710007E0

Customer Contacts