Identity
- Trade Name
- ReSolve® FDA UDI
- Generic Name
- Closed-wound drain, non-bioabsorbable FDA UDI
- Model / Reference
- 00884450146101 FDA UDI
Identifiers
- Catalog Number
- RLC40-6-038MB/B FDA UDI
- Primary DI / UDI-DI
- 00884450146101 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
Single Use
Yes
Implantable
No
Contains Latex
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
Yes
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Category: Closed-wound drain, non-bioabsorbable
ReSolve is a high-quality, single-use closed-wound drain designed for general surgery applications. It features a silicone body and comes in various sizes for orthopaedic, plastic/reconstructive, neurological, gynaecological, thoracic, cardiovascular, and general surgery uses. With its low negative pressure system, ReSolve provides efficient fluid removal and helps prevent infection.
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Authorization Coverage (1 country)
Regulatory Authorizations
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
- Merit Medical Systems, Inc.
Sources (1)
- FDA UDI 9874a460-3223-4e2d-a909-bd106ef4af19 34 fields · synced Jul 18, 2026