FDA UDI In Commercial Distribution 🇺🇸 United States

SCHWERT

DI: E89649402230 · Model: 4940-223 · A. Schweickhardt GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCHWERT
Primary DI
E89649402230
Version / Model
4940-223
Catalog Number
4940-223
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
2023-03-06
Public Version
1
Public Version Date
2023-03-14
Public Version Status
New
Public Device Record Key
695be6cb-0bf2-4d14-a30b-1c0742d3a7d5

Device Description

Crown trial forceps US-Model 17cm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
EIS REMOVER, CROWN

GMDN Terms

Code Name
64422 Dental prosthesis removal instrument

Identifiers

Type ID
Primary E89649402230

Customer Contacts