Identity
- Trade Name
- Integra® Jarit® FDA UDI
- Generic Name
- Plastic surgery file/rasp FDA UDI
- Device Name
- Integra® Jarit® Cottle Rasp, Backward Cutting FDA UDI
- Model / Reference
- 420130 FDA UDI
- Description
- Integra® Jarit® Cottle Rasp, Backward Cutting FDA UDI
Identifiers
- Catalog Number
- 420-130 FDA UDI
- Primary DI / UDI-DI
- 10381780456490 FDA UDI
- FDA Product Code
- GAC FDA UDI
- GMDN Term
- Plastic surgery file/rasp FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 7.6 Millimeter FDA UDILength — 40 Millimeter FDA UDI
Category: Plastic surgery file/rasp
Integra® Jarit® by Integra LifeSciences Production Corporation — 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
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 43fda8cc-b1de-4f7f-aa97-39e4d3943280 36 fields · synced Jun 9, 2026