Grasper Forceps, Spoon
EUDAMEDFDA UDIClass I (EU MDR)
by Joimax GmbH
Identity
- Trade Name
- Grasper Forceps, Spoon EUDAMEDForceps FDA UDI
- Generic Name
- Rigid endoscopic biopsy forceps, reusable FDA UDIRigid endoscopic tissue manipulation forceps, reusable FDA UDI
- Device Name
- Biopsy Forceps, Blakesley EUDAMEDGrasper Forceps, Spoon EUDAMEDFDA UDI
- Model / Reference
- THG242555 EUDAMEDFDA UDITHG153579 EUDAMEDFDA UDI
- Description
- Grasper Forceps, Spoon FDA UDI
Identifiers
- Catalog Number
- THG242555 FDA UDITHG153579 FDA UDI
- Primary DI / UDI-DI
- 04250337116936 EUDAMEDFDA UDI04250337120469 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371FORCGRAG8 EUDAMEDB-04250337116936 EUDAMED
- Direct Marketing DI
- 04250337120469 EUDAMED
- FDA Product Code
- GEN FDA UDI
- EMDN Code
- L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED
- GMDN Term
- Rigid endoscopic biopsy forceps, reusable FDA UDIRigid 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
Grasper Forceps, Spoon by Joimax GmbH — Class I — MDD, MDR, 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/MDD
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 42503371FORCGRAG8 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 42503371FORCGRAG8 | 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 4920ed2e-462a-43c3-8fa9-7a50be021d27 61 fields · synced Aug 4, 2026
- EUDAMED 3f024263-c6ba-46be-8505-1664095d7904 61 fields · synced May 19, 2026
- FDA UDI c7935800-298c-4ef3-823c-9867397d5d51 36 fields · synced May 30, 2026
- FDA UDI 481bc1a5-ad53-4213-85cd-fe3c64d271c7 36 fields · synced May 30, 2026
- EUDAMED f5550511-1f3f-477b-8050-459b398c8f4a 61 fields · synced Aug 1, 2026