Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Closed-wound drain, non-bioabsorbable FDA UDI
- Device Name
- DRAIN JACKSON PRATT 10MM 3/4PR FDA UDI
- Model / Reference
- SU130-1309 FDA UDI
- Description
- DRAIN JACKSON PRATT 10MM 3/4PR FDA UDI
Identifiers
- Catalog Number
- SU130-1309 FDA UDI
- Primary DI / UDI-DI
- 10192253022353 FDA UDI
- FDA Product Code
- GBX FDA UDI
- GMDN Term
- Closed-wound drain, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Closed-wound drain, non-bioabsorbable
Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Closed-wound drain, non-bioabsorbable.
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- Exodus — NAVILYST MEDICAL, INC. · Class II
- One-Step™ — Merit Medical Systems, Inc. · Class I
- Aspen® Discrete Drain — Aspen Surgical Products, 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 e7171271-621a-4e3e-9514-3621fd8c4e59 34 fields · synced Jun 8, 2026