FDA UDI In Commercial Distribution 🇺🇸 United States

SCHWERT

DI: E89617061130 · Model: 1706-113 · A. Schweickhardt GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCHWERT
Primary DI
E89617061130
Version / Model
1706-113
Catalog Number
1706-113
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
2023-02-21
Public Version
1
Public Version Date
2023-03-01
Public Version Status
New
Public Device Record Key
1182d53f-5241-432a-91f8-a7b428943879

Device Description

Periotome PER 3

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
EMK CURETTE, SURGICAL, DENTAL

GMDN Terms

Code Name
38168 Periosteal elevator, reusable

Identifiers

Type ID
Primary E89617061130

Customer Contacts