FDA UDI In Commercial Distribution 🇺🇸 United States

TEKNO®

DI: 04044684066378 · Model: 50459-08 · Tekno-Medical Optik-Chirurgie GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TEKNO®
Primary DI
04044684066378
Version / Model
50459-08
Catalog Number
50459-08
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
2022-10-11
Public Version
1
Public Version Date
2022-10-19
Public Version Status
New
Public Device Record Key
f4b1c8a7-d4ef-40a7-a4ce-bafde4cb97fd

Device Description

HARTMANN EAR FORCEPS 8,5CM

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
KAE Forceps, Ent

GMDN Terms

Code Name
62467 Surgical soft-tissue manipulation forceps, alligator, reusable

Identifiers

Type ID
Primary 04044684066378

Customer Contacts

Phone
+49746117010