FDA UDI In Commercial Distribution 🇺🇸 United States

Tourniquet Silicone Cuff; Double Cuff

DI: 14250105630050 · Model: 20-60-722 · VBM Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Tourniquet Silicone Cuff; Double Cuff
Primary DI
14250105630050
Version / Model
20-60-722
Company Name
VBM Medizintechnik GmbH
Labeler DUNS
324869601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-27
Public Version
1
Public Version Date
2024-07-05
Public Version Status
New
Public Device Record Key
2a0059fa-2756-4383-b5f2-70249b16adf2

Device Description

61 cm / 24 inch

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KCY Tourniquet, Pneumatic

GMDN Terms

Code Name
17230 Tourniquet cuff, reusable

Identifiers

Type ID
Direct Marking 04250105630053
Primary 14250105630050
Previous 04250105606942

Customer Contacts

Phone
+49745495960

Device Sizes

Type Value Unit Text
Length 61 Centimeter
Length 24 Inch

Storage Conditions

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