gudid
Primary ID: 6837-1
KINESIOLOGY TAPE PRE-CUT ROLL (UDI 6837-1)
Manufactured by Mueller Sports Medicine, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KINESIOLOGY TAPE PRE-CUT ROLL - Primary ID 6837-1
Device Regulatory Overview
The KINESIOLOGY TAPE PRE-CUT ROLL (Model/Catalog Number: 6837-1) is a medical device manufactured by Mueller Sports Medicine, Inc.. This product is indexed under FDA Product Code / Category Classification FQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6837-1
- Product Code / EMDN
- FQM
- Device Name
- KINESIOLOGY TAPE PRE-CUT ROLL BLUE
- Database Sync Date
- 2026-08-09 09:08:47
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of KINESIOLOGY TAPE PRE-CUT ROLL?
The registered manufacturer of record for KINESIOLOGY TAPE PRE-CUT ROLL is Mueller Sports Medicine, Inc..
What is the Primary UDI-DI identifier for KINESIOLOGY TAPE PRE-CUT ROLL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6837-1.
What classification code is assigned to this device?
This device is registered under product classification code FQM.
Similar Classification Devices (FQM)
Other Devices by Mueller Sports Medicine, Inc.
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