Identity
- Trade Name
- Curity FDA UDI
- Generic Name
- Suture kit, medicated FDA UDI
- Device Name
- Laceration Set FDA UDI
- Model / Reference
- 99018 FDA UDI
- Description
- Laceration Set FDA UDI
Identifiers
- Catalog Number
- 99018 FDA UDI
- Primary DI / UDI-DI
- 10884521069848 FDA UDI
- FDA Product Code
- KDD FDA UDI
- GMDN Term
- Suture kit, medicated FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Suture kit, medicated
Curity by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- Sterling Medical Products — APOLLO MEDICAL PRODUCTS CORP.
- Syneture — Covidien LP · Class II
- Regard™ — RESOURCE OPTIMIZATION & INNOVATION, L.L.C. · Class II
- Hayden Medical — Hayden Medical 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
- Cardinalhealth
Sources (1)
- FDA UDI 83a77056-c521-4525-8bbe-490772344f23 36 fields · synced May 30, 2026