Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Skin-closure adhesive strip FDA UDI
- Device Name
- Wound Closure Strips; Reinforced; 1/8 in. x 3 in. FDA UDI
- Model / Reference
- S1040 FDA UDI
- Description
- Wound Closure Strips; Reinforced; 1/8 in. x 3 in. FDA UDI
Identifiers
- Catalog Number
- S1040 FDA UDI
- Primary DI / UDI-DI
- 00885380027850 FDA UDI
- FDA Product Code
- NAD FDA UDI
- GMDN Term
- Skin-closure adhesive strip FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4020 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
Yes
FDA UDI
Over-the-Counter
No
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Skin-closure adhesive strip
Cardinal Health by Cardinal Health 200, LLC — 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
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- 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
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 315f1cf2-9844-4baf-a5e4-bf39a40e8f39 34 fields · synced Jun 8, 2026