FDA UDI In Commercial Distribution 🇺🇸 United States

TEKNO®

DI: 04044684076490 · Model: 70105-03MD · Tekno-Medical Optik-Chirurgie GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
TEKNO®
Primary DI
04044684076490
Version / Model
70105-03MD
Catalog Number
70105-03MD
Company Name
Tekno-Medical Optik-Chirurgie GmbH
Labeler DUNS
318762069
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-18
Public Version
1
Public Version Date
2022-10-26
Public Version Status
New
Public Device Record Key
95f9494b-ed40-44d5-be43-9f44e859b949

Device Description

MEAD EXTR. FORCEPS, ENGL.PATT.,FIG. MD3

Device Characteristics

Single Use
No
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
EMG Forceps, Tooth Extractor, Surgical

GMDN Terms

Code Name
35552 Tooth extraction forceps

Identifiers

Type ID
Primary 04044684076490

Customer Contacts

Phone
+49746117010