Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Neurosurgical retraction system, spinal FDA UDI
- Device Name
- Scoville Retractor, blade, solid, blade length 100mm, blade width 25mm FDA UDI
- Model / Reference
- IPN920557 FDA UDI
- Description
- Scoville Retractor, blade, solid, blade length 100mm, blade width 25mm FDA UDI
Identifiers
- Catalog Number
- P22363 FDA UDI
- Primary DI / UDI-DI
- 14026704726131 FDA UDI
- FDA Product Code
- GZT FDA UDI
- GMDN Term
- Neurosurgical retraction system, spinal FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 46 Millimeter FDA UDIHeight — 26 Millimeter FDA UDILength — 100 Millimeter FDA UDI
Category: Neurosurgical retraction system, spinal
Pilling by Teleflex Incorporated — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 4aa31f69-0fdc-49d0-9f17-d6fdd2be30bb 36 fields · synced Jun 6, 2026