Wang
by Conmed Corporation United States EUDAMEDGUDID
Ref SW-221, MW-222, SW-121, MWF-319, MW-319, MW-322, MW-122, W-220
Product code EOQEMDN A01020502
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-20653405052699 | Date3 Apr 2026 | StatusActive |
| United States | GUDID listing GUDID | Number20653405052699 | Date24 Sep 2016 | StatusIn distribution |
Coverage
- Expiring (legacy directive)
- Listed
- Not covered
- European Union
- United States
Recalls
-
- Terminated Z-0504-2013
- Terminated Z-0502-2013
- Terminated Z-0505-2013
- Terminated Z-0503-2013
ConMed received complaints from a user facility reporting that the WANG Transbronchial Aspiration Needles would not insert properly through the instrument channel of a 2.0 mm bronchoscope. If the device will not fit through the instrument channel of a 2.0 mm bronchoscope, it must be replaced with an alternate device and could result in minor inconvenience to the user.
Specification
- Generic Name
- Body aspiration needle, single-use
- Device Name
- Non-orthopedic, Non-active, Needle, Aspiration
- Model / Ref / Catalog
- SW-221, MW-222, SW-121, MWF-319, MW-319, MW-322, MW-122, W-220
- Primary DI / UDI-DI
- 20653405052699, 20653405052651, 20653405052682, 20653405052736, 20653405052729, 20653405052668, 20653405052644, 20653405052712
- Basic UDI-DI
- B-20653405052699, B-20653405052651, B-20653405052682, B-20653405052736, B-20653405052729, B-20653405052668, B-20653405052644, B-20653405052712
- 510(k) Number
- FDA Product Code
- EOQ
- EMDN Code
- A01020502 Laparoscopic and thoracoscopic biopsy needles and kits
- GMDN Term
- Body aspiration needle, single-use
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 874.4680
- Market of Registration
- Belgium
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Ethylene Oxide
- Size
- Outer Diameter — 1.9 MillimeterLength — 130 CentimeterLength — 15 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- US-MF-000012663
- Authorised representative
- MDSS GmbH DE-AR-000005430
Other devices from Conmed Corporation
Properties & raw data
Show properties, registry sources and raw records
Other properties (19)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No
Sources (16)
- EUDAMED 6c9b14e2-4f4a-4c63-9996-8fb4fb60f973
- EUDAMED 20653405052651|B-20653405052651
- EUDAMED 20653405052682|B-20653405052682
- EUDAMED 20653405052736|B-20653405052736
- EUDAMED 20653405052729|B-20653405052729
- EUDAMED 20653405052668|B-20653405052668
- EUDAMED 20653405052644|B-20653405052644
- EUDAMED 20653405052712|B-20653405052712
- FDA UDI 9a60f876-4c16-4909-8772-3ee87e00c3ac
- FDA UDI d9ebae94-ead1-4a45-a243-74f564959cf9
- FDA UDI f567d080-120e-4003-b0d0-5863f457d859
- FDA UDI 24a49775-6400-4a46-8f10-a309972268b4
- FDA UDI 68ce19a1-c24c-43f1-875f-7efc3565581a
- FDA UDI e684604c-c035-40ef-adee-3738e53c44fe
- FDA UDI 94089adf-eae5-4239-9fa6-f8075859fefd
- FDA UDI 14bf3290-af70-443a-9cfb-f6aed9188799