Identity
- Trade Name
- Millennium FDA UDI
- Generic Name
- Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
- Device Name
- Poole Suction, 3-piece take apart, 3 3/4" removable 2-piece fenestrated tip, 4" knurled handle with barbed tube fitting, 8 3/8" OL FDA UDI
- Model / Reference
- 72-242405RSD FDA UDI
- Description
- Poole Suction, 3-piece take apart, 3 3/4" removable 2-piece fenestrated tip, 4" knurled handle with barbed tube fitting, 8 3/8" OL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190776377212 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Surgical irrigation/aspiration cannula, non-illuminating, reusable 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
Category: Surgical irrigation/aspiration cannula, non-illuminating, reusable
Millennium by AVALIGN TECHNOLOGIES, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical irrigation/aspiration cannula, non-illuminating, reusable.
- FENTEX — FENTEX medical GmbH · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Laryngeal cannula — Spiggle & Theis Medizintechnik GmbH · Class I
- Cannula, Suction, acc. Anthony 27.0cm long Ø4mm Charr./Fr. 12 with cone — Geister Medizin Technik GmbH · Class I
- Verhoeven suction tube — Spiggle & Theis Medizintechnik GmbH · Class I
- Modulap — ATC TECHNOLOGIES INC. · Class II
- CANNULA — SONTEC INSTRUMENTS, INC. · Class I
- Cannula, Suction, acc. Braun-Ralph spare part suction tip — Geister Medizin Technik GmbH · Class I
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
- AVALIGN TECHNOLOGIES, Inc.
Sources (1)
- FDA UDI 25f555a6-2e1b-4748-823b-8dedcdcb2d9d 34 fields · synced May 31, 2026