Semi-Flexible Grasper Forceps, curved, up-biting
EUDAMEDFDA UDIClass I (EU MDR)
by Joimax GmbH
Identity
- Trade Name
- Semi-Flexible Grasper Forceps, curved, up-biting EUDAMEDForceps FDA UDI
- Generic Name
- Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
- Device Name
- Semi-Flexible Grasper Forceps, curved, up-biting EUDAMEDFDA UDISemi-Flexible Grasper Forceps EUDAMED
- Model / Reference
- TFG322522U EUDAMEDFDA UDITFG352522U EUDAMEDFDA UDI
- Description
- Semi-Flexible Grasper Forceps, curved, up-biting FDA UDI
Identifiers
- Catalog Number
- TFG352522U FDA UDITFG322522U FDA UDI
- Primary DI / UDI-DI
- 04250337105435 EUDAMEDFDA UDI04250337103592 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337105435 EUDAMED42503371FORCSEMHM EUDAMED
- Direct Marketing DI
- 04250337103592 EUDAMED
- FDA Product Code
- GEN FDA UDI
- EMDN Code
- L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED
- GMDN Term
- Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
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
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: Flexible endoscopic biopsy forceps, reusable
Semi-Flexible Grasper Forceps, curved, up-biting by Joimax GmbH — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible endoscopic biopsy forceps, reusable.
- Laryngoscopy Forceps — SONTEC INSTRUMENTS, INC. · Class I
- STRATTE SCISSORS — SONTEC INSTRUMENTS, INC. · Class I
- ELMED INCORPORATED — ELMED INCORPORATED · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Laryngoscopy Forceps — SONTEC INSTRUMENTS, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
CE/MDD
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-04250337105435 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-04250337105435 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (5)
- EUDAMED 81f5ead9-58bc-4520-892e-2532708042f4 61 fields · synced Jul 22, 2026
- EUDAMED e834a960-eb27-4252-8b91-7b5365e8b1b1 61 fields · synced May 19, 2026
- FDA UDI f518e4cf-77aa-47a8-981f-df35eb4559fe 36 fields · synced May 29, 2026
- FDA UDI 8e580d2c-1f03-4e0e-bafd-3a9c34bf47f6 36 fields · synced May 30, 2026
- EUDAMED cd239147-4228-4e57-8c8a-f72a226ca0e9 61 fields · synced Jul 22, 2026