FDA UDI In Commercial Distribution 🇺🇸 United States

KindKlamp

DI: 00653599002179 · Model: 20003CA · BIODERM, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KindKlamp
Primary DI
00653599002179
Version / Model
20003CA
Company Name
BIODERM, INC.
Labeler DUNS
114773653
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-07
Public Version
1
Public Version Date
2024-02-15
Public Version Status
New
Public Device Record Key
8cf3e691-bf79-4549-a513-8609487a1bd4

Device Description

KindKlamp, Penile Clamp, Canada

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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FHA Clamp, Penile

GMDN Terms

Code Name
42797 Incontinence penis clamp, reusable

Identifiers

Type ID
Primary 00653599002179

Customer Contacts

Phone
800-864-6755

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius