FDA UDI In Commercial Distribution 🇺🇸 United States

n.a.

DI: 04250105619232 · Model: 23-00-722 · VBM Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
n.a.
Primary DI
04250105619232
Version / Model
23-00-722
Company Name
VBM Medizintechnik GmbH
Labeler DUNS
324869601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-14
Public Version
2
Public Version Date
2023-08-31
Public Version Status
Update
Public Device Record Key
5e6bb06a-7027-4602-8627-f2d8fa4878da

Device Description

Tourniquet Sleeve

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
KCY Tourniquet, Pneumatic

GMDN Terms

Code Name
47949 Tourniquet cuff bandage, non-latex

Identifiers

Type ID
Package 14250105619239
Primary 04250105619232

Customer Contacts

Phone
+49745495960

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry, Keep away from sunlight and heat