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TESSYS® Grasper Forceps, 2-1 toothing
EUDAMEDFDA UDIClass I (EU MDR)
Ref TFG323021
by Joimax GmbH
Identity
- Trade Name
- TESSYS® Grasper Forceps, 2-1 toothing EUDAMEDForceps FDA UDI
- Generic Name
- Rigid endoscopic biopsy forceps, reusable FDA UDI
- Device Name
- Biopsy Forceps, Blakesley EUDAMEDTESSYS® Grasper Forceps, 2-1 toothing EUDAMEDFDA UDI
- Model / Reference
- TFG323021 EUDAMEDFDA UDI
- Description
- TESSYS® Grasper Forceps, 2-1 toothing FDA UDI
Identifiers
- Catalog Number
- TFG323021 FDA UDI
- Primary DI / UDI-DI
- 04250337114871 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371FORCGRAG8 EUDAMEDB-04250337114871 EUDAMED
- FDA Product Code
- GEN FDA UDI
- EMDN Code
- L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED
- GMDN Term
- Rigid endoscopic biopsy 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
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
TESSYS® Grasper Forceps, 2-1 toothing by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
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 |
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Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (3)
- EUDAMED 9c092c1c-4039-439f-8e37-dc7ca6bd311e 61 fields · synced Jul 19, 2026
- EUDAMED 752beda1-7f3c-4c96-a486-cb9d551c339d 61 fields · synced May 18, 2026
- FDA UDI a3ccc7be-b834-42dc-9e8a-a506ac07fafb 36 fields · synced May 30, 2026