Identity
- Trade Name
- SENSATION FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- SENSATION Micro Forceps, straight, 7 1/2", (190 mm), working length: 2 3/4", (70 mm), bayonet-shaped, round plastic handle, width: 0,500 mm, black, non-sterile, reusable FDA UDI
- Model / Reference
- FM150R FDA UDI
- Description
- SENSATION Micro Forceps, straight, 7 1/2", (190 mm), working length: 2 3/4", (70 mm), bayonet-shaped, round plastic handle, width: 0,500 mm, black, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- FM150R FDA UDI
- Primary DI / UDI-DI
- 04038653201129 FDA UDI
- FDA Product Code
- GZX FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 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
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Sensation by Aesculap, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, reusable.
- Micro-Pliers 17, 5 cm, lightweight, DCL coated — SALVIN DENTAL SPECIALTIES, LLC · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- STILLE Titanium Micro Forceps — Stille AB · Class I
- Gen2 — SURGIX MEDICAL LLC · Class I
- TISSUE FORCEPS SEMKEN 6" SERRATED STRAIGHT — W.H. Holden, Inc. · Class I
- V. Mueller — STERIS CORPORATION · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · 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
- Aesculap, Inc.
Sources (1)
- FDA UDI a439f65b-35cc-4b31-ae56-6b74d53972b4 35 fields · synced Jun 8, 2026