← Back to catalogue
Antrum Punch, Backward Cutting, Rotatable, 8x2.5mm Bite, 10cm WL
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Antrum Punch, Backward Cutting, Rotatable, 8x2.5mm Bite, 10cm WL FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
- Device Name
- Actuated Cutting FDA UDI
- Model / Reference
- 07-181-15MA FDA UDI
- Description
- Actuated Cutting FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810009460978 FDA UDI
- FDA Product Code
- LRY FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Category: Surgical soft-tissue manipulation forceps, alligator, reusable
Antrum Punch, Backward Cutting, Rotatable, 8x2.5mm Bite, 10cm WL by Mizuho America, Inc. — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Surgical soft-tissue manipulation forceps, alligator, reusable.
- Integra® — Integra LifeSciences Production Corporation · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- Symmetry Goodhill — SYMMETRY SURGICAL INC. · Class I
- JEDMED — JEDMED Instrument Company · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Micro laryngeal forceps — Spiggle & Theis Medizintechnik GmbH · Class I
- Symmetry Jako — SYMMETRY SURGICAL INC. · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mizuho America, Inc.
Sources (1)
- FDA UDI 5d8ef7ab-ae24-4f20-b5e2-747c9062c5e1 33 fields · synced Jun 1, 2026