← Back to catalogue
joimax® Needle 21G, Pencil Point, graduated
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref JMSN21G
by Joimax GmbH
Identity
- Trade Name
- joimax® Needle 21G, Pencil Point, graduated EUDAMEDN/A FDA UDI
- Generic Name
- Hypodermic needle, single-use FDA UDI
- Device Name
- joimax® Needle 21G, Pencil Point, graduated EUDAMEDFDA UDIjoimax® Needle 21G, Pencil Point EUDAMED
- Model / Reference
- JMSN21G EUDAMEDFDA UDI
- Description
- joimax® Needle 21G, Pencil Point, graduated FDA UDI
Identifiers
- Catalog Number
- JMSN21G FDA UDI
- Primary DI / UDI-DI
- 04250337100775 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337100775 EUDAMED42503371ACNENPP9L EUDAMED
- Direct Marketing DI
- 04250337100775 EUDAMED
- FDA Product Code
- GAA FDA UDI
- EMDN Code
- A01030101 SPINAL ANAESTHESIA NEEDLES AND KITS EUDAMED
- GMDN Term
- Hypodermic needle, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- 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
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
joimax® Needle 21G, Pencil Point, graduated by Joimax GmbH — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-04250337100775 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-04250337100775 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (3)
- EUDAMED 4bc4e913-bf0c-4c1e-b7e9-9ff5f11384c6 61 fields · synced Jul 22, 2026
- FDA UDI ff482d1d-109d-453a-bb75-e9e3c6b3972a 36 fields · synced May 30, 2026
- EUDAMED 74eb1591-df92-4dbd-89c6-56154c05c719 61 fields · synced Jun 20, 2026