gudid
Primary ID: TS-001
T-STRIP (UDI TS-001)
Manufactured by PRECISION MEDICAL DEVICES, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for T-STRIP - Primary ID TS-001
Device Regulatory Overview
The T-STRIP (Model/Catalog Number: TS-001) is a medical device manufactured by PRECISION MEDICAL DEVICES, LLC. This product is indexed under FDA Product Code / Category Classification MGO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TS-001
- Product Code / EMDN
- MGO
- Device Name
- The T-Strip is a 2.0 X 7.5 cm porous mesh wound closure strip that allows quick, and easy approximation of the edges of traumatic wounds; while reducing wound tension. The transparent T-Strip allows ideal wound approximation; simply apply to one side of the wound, then gently pull across the wound while aligning the edges. Adhere the remaining adhesive mesh to the other side of the wound, then apply a topical skin adhesive (skin glue) directly on and through the T-strip, sealing the wound.
- Database Sync Date
- 2026-08-09 09:49:14
Full Regulatory Attributes
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{
"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 T-STRIP?
The registered manufacturer of record for T-STRIP is PRECISION MEDICAL DEVICES, LLC.
What is the Primary UDI-DI identifier for T-STRIP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TS-001.
What classification code is assigned to this device?
This device is registered under product classification code MGO.
Similar Classification Devices (MGO)
Other Devices by PRECISION MEDICAL DEVICES, LLC
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