Identity
- Trade Name
- Needle EUDAMEDMaxiCell™ Biopsy Needle FDA UDI
- Generic Name
- Body aspiration needle, single-use FDA UDI
- Device Name
- MaxiCell Biopsy Needle EUDAMEDMaxiCell™ Biopsy Needle 22ga x 5cm FDA UDI
- Model / Reference
- MMC2202 EUDAMEDFDA UDI
- Description
- MaxiCell™ Biopsy Needle 22ga x 5cm FDA UDI
Identifiers
- Catalog Number
- MMC2202 FDA UDI
- Primary DI / UDI-DI
- 20886333002812 EUDAMED00886333002818 FDA UDI
- Basic UDI-DI
- B-20886333002812 EUDAMED
- 510(k) Number
- K980122 FDA UDI
- FDA Product Code
- KNW FDA UDI
- EMDN Code
- A01020102 ASPIRATION FINE NEEDLES AND KITS EUDAMED
- GMDN Term
- Body aspiration needle, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1075 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Diskectomy system, percutaneous, automatic
Needle by Argon Medical Devices, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as Diskectomy system, percutaneous, automatic.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-20886333002812 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Argon Medical Devices, Inc.
- EUDAMED SRN
- US-MF-000002324
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED de196049-9b2c-4eec-b79d-ea2c7913384b 61 fields · synced Jul 28, 2026
- FDA UDI c1c09dd0-8e10-4f84-a94b-7c5d1ee4d2d6 39 fields · synced May 30, 2026