Identity
- Trade Name
- MicroFrance® FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
- Device Name
- MicroFrance® Itard eustachian catheter probe, Size 3 FDA UDI
- Model / Reference
- 7722-3 FDA UDI
- Description
- MicroFrance® Itard eustachian catheter probe, Size 3 FDA UDI
Identifiers
- Catalog Number
- 7722-3 FDA UDI
- Primary DI / UDI-DI
- 10381780538509 FDA UDI
- FDA Product Code
- KAK 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 UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Surgical/emergency suction cannula, non-illuminating, reusable
MicroFrance is a reliable, reusable surgical/emergency suction cannula designed for accurate aspiration and observation of body cavities, wounds, or surgical sites. Its single-lumen design facilitates clear visualization, while the non-illuminating feature ensures patient comfort. MicroFrance is a versatile device suitable for various medical specialties, including ENT, otolaryngology, and oral surgery.
Similar devices
Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- Ambler Surgical — Ambler Surgical, LLC · Class II
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- SCANLAN® Variable Suction Rotatable Tips — SCANLAN INTERNATIONAL INC · Class I
- Fukushima Tear Drop Suction Tube Straight Malleable 10 Fr. 21 cm - 8 1/4" Ø 3.3 mm — SURTEX INSTRUMENTS LTD · Class IIa
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class II
- LAZIC — Peter Lazic GmbH · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
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 Microfrance
Sources (1)
- FDA UDI d34c3012-b25b-4a42-ab78-b1118e344577 35 fields · synced Jun 26, 2026