Identity
- Trade Name
- Marina Medical FDA UDI
- Generic Name
- Open-surgery biopsy forceps, reusable FDA UDI
- Device Name
- Tischler Biopsy Forceps, 3mm x 7mm Jaw, 20cm FDA UDI
- Model / Reference
- 290-208 FDA UDI
- Description
- Tischler Biopsy Forceps, 3mm x 7mm Jaw, 20cm FDA UDI
Identifiers
- Catalog Number
- 290-208 FDA UDI
- Primary DI / UDI-DI
- 00840306806919 FDA UDI
- FDA Product Code
- HFB FDA UDI
- GMDN Term
- Open-surgery biopsy forceps, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Safe FDA UDI
Category: Open-surgery biopsy forceps, reusable
Marina Medical by Marina Medical Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- ARTHROSCOPIC GRASPING RONGEUR FORCEPS — SONTEC INSTRUMENTS, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Marina Medical Instruments, Inc.
Sources (1)
- FDA UDI 5d43ad50-7ee8-455e-a72d-aa690e9c6e1d 35 fields · synced Jun 1, 2026