FDA UDI In Commercial Distribution 🇺🇸 United States

KaWe

DI: 00845821020840 · Model: 61-848-010 · BV Medical
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KaWe
Primary DI
00845821020840
Version / Model
61-848-010
Company Name
BV Medical
Labeler DUNS
105932508
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
4c4d2310-932b-4d20-9d41-233aac18d338

Device Description

3.5mm Reusable Specula for KaWe COMBILIGHT®

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
Yes
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
No

Product Codes

Code Name
FXG Specula Accessories

GMDN Terms

Code Name
33395 Ear speculum, reusable

Identifiers

Type ID
Primary 00845821020840

Customer Contacts