Identity
- Trade Name
- Combine Pads FDA UDI
- Generic Name
- Absorbent wound compression pad FDA UDI
- Device Name
- Combine Pads 1/Pouch- Sterile, 5"x9" FDA UDI
- Model / Reference
- 3501 FDA UDI
- Description
- Combine Pads 1/Pouch- Sterile, 5"x9" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00616784350110 FDA UDI
- FDA Product Code
- FRL FDA UDINAB FDA UDI
- GMDN Term
- Absorbent wound compression pad FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5300 FDA UDI878.4014 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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Absorbent wound compression pad
Combine Pads by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Absorbent wound compression pad.
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- HK Non-Sterile Super Absorbent Pads Large — HK SURGICAL INC. · Class I
- HK Sterile Super Absorbent Pads Large — HK SURGICAL INC. · Class I
- HK Sterile Super Absorbent Pads Small — HK SURGICAL INC. · Class I
- HK Non-Sterile Super Absorbent Pads XL — HK SURGICAL INC. · Class I
- ASP MEDICAL — Asp Global, LLC · Class I
- HK Non-Sterile Super Absorbent Pads Medium — HK SURGICAL 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
- Dynarex Corp.
Sources (1)
- FDA UDI 17f4c850-86e2-4a52-8ef8-d3da8f1e149a 33 fields · synced Jun 8, 2026