FDA UDI In Commercial Distribution 🇺🇸 United States

PRESTIGEPRO

DI: 00840490800021 · Model: 6421 · PRESTIGE AMERITECH, LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PRESTIGEPRO
Primary DI
00840490800021
Version / Model
6421
Catalog Number
6421
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-04
Public Version
1
Public Version Date
2025-04-14
Public Version Status
New
Public Device Record Key
d048d44f-de5b-41bc-89ea-2989f22a5e91

Device Description

Stretch Tourniquets, 1in x 18in, Orange, Single Use, Non-Sterile, Textured, 250 per box

Device Characteristics

Single Use
Yes
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
GAX Tourniquet, Nonpneumatic

GMDN Terms

Code Name
67048 Venous tourniquet, single-use

Identifiers

Type ID
Package 10840490800028
Primary 00840490800021

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry, avoid direct sunlight