Identity
- Trade Name
- Draf ethmoid forceps FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
- Device Name
- 90° angled 6x2.4 mm, 13 cm FDA UDI
- Model / Reference
- 30-724-13 FDA UDI
- Description
- 90° angled 6x2.4 mm, 13 cm FDA UDI
Identifiers
- Catalog Number
- 30-724-13 FDA UDI
- Primary DI / UDI-DI
- 04250381814390 FDA UDI
- FDA Product Code
- LRC FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical soft-tissue manipulation forceps, alligator, reusable
Draf ethmoid forceps by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Symmetry Jako — SYMMETRY SURGICAL INC. · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc. · Class II
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
- Spiggle & Theis Medizintechnik GmbH
Sources (1)
- FDA UDI 1aff361b-429c-4b0a-ae44-a2822c736b9d 35 fields · synced May 29, 2026