FDA UDI In Commercial Distribution 🇺🇸 United States

ERMIS

DI: 04049224294686 · Model: ER200.030VA · Ermis MedTech GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ERMIS
Primary DI
04049224294686
Version / Model
ER200.030VA
Catalog Number
ER200.030VA
Company Name
Ermis MedTech GmbH
Labeler DUNS
313118522
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-07
Public Version
1
Public Version Date
2025-10-15
Public Version Status
New
Public Device Record Key
f1856adf-c927-48c0-81c2-8669f43e88f6

Device Description

3/4 Premium Lid perforated, red, 462x280 mm, valve system

Device Characteristics

Single Use
No
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
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
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04049224294686

Customer Contacts