Identity
- Trade Name
- Integra® MicroFrance® FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
- Device Name
- LOANER Stamm Skull Base Instrument Kit FDA UDI
- Model / Reference
- MCEN320LP FDA UDI
- Description
- LOANER Stamm Skull Base Instrument Kit FDA UDI
Identifiers
- Catalog Number
- MCEN320LP FDA UDI
- Primary DI / UDI-DI
- 10381780490418 FDA UDI
- FDA Product Code
- KBD FDA UDIKAD FDA UDIKAK FDA UDIJZF FDA UDIGDG FDA UDIMMO FDA UDIGEI FDA UDIKAE FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 FDA UDI878.4800 FDA UDI878.4400 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Instrument tray, reusableGeneral-purpose surgical scissors, reusableElectrical-only medical device connection cable, reusableSurgical/emergency suction cannula, non-illuminating, reusable
Integra® MicroFrance® 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 1e2adaad-b3bb-4025-9581-537259737a5b 35 fields · synced Jun 9, 2026