Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
- Device Name
- CURAPLEX RUSSELL DECOMPRESSION NEEDLE, PNEUMOFIX, 12 GA FDA UDI
- Model / Reference
- PDF112 FDA UDI
- Description
- CURAPLEX RUSSELL DECOMPRESSION NEEDLE, PNEUMOFIX, 12 GA FDA UDI
Identifiers
- Catalog Number
- PDF112 FDA UDI
- Primary DI / UDI-DI
- 00810071636059 FDA UDI
- FDA Product Code
- GCB FDA UDI
- GMDN Term
- Spring-loaded pneumoperitoneum needle, single-use 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Length — 11 Centimeter FDA UDI
Category: Spring-loaded pneumoperitoneum needle, single-use
Curaplex by Bound Tree Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI bd2ed6e8-85fd-4626-a16e-f9ededf0401d 35 fields · synced May 30, 2026