Identity
- Trade Name
- PEAK MEDICAL FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- Halstead Forceps - Curved serrated jaws w/1x2 teeth, Titanium, 4.75" (12.5cm) FDA UDI
- Model / Reference
- 511-0858.22 FDA UDI
- Description
- Halstead Forceps - Curved serrated jaws w/1x2 teeth, Titanium, 4.75" (12.5cm) FDA UDI
Identifiers
- Primary DI / UDI-DI
- G4535110858220 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, 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
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
No
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
No
Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable
At Peak Medical, we offer a range of high-quality surgical instruments designed to facilitate precise and effective soft-tissue manipulation during medical procedures. The Halstead Forceps - Curved serrated jaws w/1x2 teeth, Titanium, 4.75" (12.5cm) is a versatile instrument suitable for a variety of applications in general surgery, plastic surgery, and ophthalmic surgery. With its durable design, comfortable grip, and precision-engineered features, this forceps is an excellent choice for medical professionals seeking reliable and efficient instrumentation.
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
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
- PEAK MEDICAL Distribution Inc
Sources (1)
- FDA UDI 3031c123-4e32-4bca-8e74-0b17479597d3 33 fields · synced Jul 8, 2026