FDA UDI In Commercial Distribution 🇺🇸 United States

TEKNO®

DI: 04044684079934 · Model: 71028-13 · Tekno-Medical Optik-Chirurgie GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TEKNO®
Primary DI
04044684079934
Version / Model
71028-13
Catalog Number
71028-13
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
7105c44a-1fd0-4598-985e-324b65481561

Device Description

STIEGLITZ SPLINTER FORCEPS 90'

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
EFL Forceps, Dressing, Dental

GMDN Terms

Code Name
35552 Tooth extraction forceps

Identifiers

Type ID
Primary 04044684079934

Customer Contacts

Phone
+49746117010