Identity
- Trade Name
- T-STRIP FDA UDI
- Generic Name
- Skin-closure adhesive strip FDA UDI
- 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. FDA UDI
- Model / Reference
- TS-001 FDA UDI
- Description
- 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. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00869193000002 FDA UDI
- FDA Product Code
- MGO FDA UDI
- GMDN Term
- Skin-closure adhesive strip FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4018 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Radiation Sterilization FDA UDI
Category: Skin-closure adhesive strip
T-Strip by Precision Medical Devices Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin-closure adhesive strip.
- UC Strip™ — Derma Sciences Canada, Inc · Class I
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- Suture Strip® — Derma Sciences Canada, Inc · Class I
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- BContak — BRIDON, CORP. · Class III
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- CareOne — Ahold U.S.A., Inc. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Precision Medical Devices Inc
Sources (1)
- FDA UDI 18b268b8-0888-4a0c-b399-1f3fdf279aa3 34 fields · synced Jun 8, 2026