FDA UDI In Commercial Distribution 🇺🇸 United States

Otoform® Ak X

DI: E2394751 · Model: 475 · Dreve Otoplastik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Otoform® Ak X
Primary DI
E2394751
Version / Model
475
Catalog Number
475
Company Name
Dreve Otoplastik GmbH
Labeler DUNS
315808340
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-12
Public Version
1
Public Version Date
2022-08-22
Public Version Status
New
Public Device Record Key
26b718c9-01ce-44c6-9220-bfd84f28646b

Device Description

No.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LDG Kit, earmold, impression

GMDN Terms

Code Name
43783 Earmould impression kit

Identifiers

Type ID
Primary E2394751

Customer Contacts

Phone
+49230388070

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
18 – 28 Degrees Celsius