FDA UDI In Commercial Distribution 🇺🇸 United States

N.A.

DI: 04049368060369 · Model: 15921 · Geuder Aktiengesellschaft
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N.A.
Primary DI
04049368060369
Version / Model
15921
Catalog Number
15921
Company Name
Geuder Aktiengesellschaft
Labeler DUNS
316267202
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-23
Public Version
1
Public Version Date
2021-03-03
Public Version Status
New
Public Device Record Key
44625776-c54e-47a8-818f-3345d0619ccc

Device Description

N.A.

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
No
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
HNC Specula, ophthalmic

GMDN Terms

Code Name
35349 Eyelid speculum, reusable

Identifiers

Type ID
Primary 04049368060369