FDA UDI In Commercial Distribution 🇺🇸 United States

ER802.000N

DI: 04049224309069 · Model: ER802.000N · Ermis MedTech GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ER802.000N
Primary DI
04049224309069
Version / Model
ER802.000N
Catalog Number
ER802.000N
Company Name
Ermis MedTech GmbH
Labeler DUNS
313118522
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-21
Public Version
6
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
7d940c98-fc43-40a4-a3b6-55dcd7435d64

Device Description

Single use paper filter, 100 Pcs/Package

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04049224309069

Customer Contacts