Identity
- Trade Name
- Centurion FDA UDI
- Generic Name
- General surgical procedure kit, medicated FDA UDI
- Device Name
- CENTRAL LINE DRESSING KIT FDA UDI
- Model / Reference
- DT20240 FDA UDI
- Description
- CENTRAL LINE DRESSING KIT FDA UDI
Identifiers
- Catalog Number
- DT20240 FDA UDI
- Primary DI / UDI-DI
- 10653160292098 FDA UDI
- FDA Product Code
- OXQ FDA UDI
- GMDN Term
- General surgical procedure kit, medicated FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5075 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
Yes
FDA UDI
Combination Product
Yes
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: General surgical procedure kit, medicated
Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
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
- Centurion Medical Products
Sources (1)
- FDA UDI 4d8f9eec-ca91-4c9b-88f1-02b918ded768 35 fields · synced Jun 1, 2026