Identity
- Trade Name
- Surgical Direct FDA UDI
- Generic Name
- Laparoscopic tissue manipulation forceps/working-channel FDA UDI
- Device Name
- 5mm 32cm Micro Dissecting Forcep, Double Action, 13.5mm Jaw Length, Monopolar Rotatable Handle, with FDA UDI
- Model / Reference
- SD8918-900 FDA UDI
- Description
- 5mm 32cm Micro Dissecting Forcep, Double Action, 13.5mm Jaw Length, Monopolar Rotatable Handle, with FDA UDI
Identifiers
- Catalog Number
- SD8918-900 FDA UDI
- Primary DI / UDI-DI
- B382SD89189000 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Laparoscopic tissue manipulation forceps/working-channel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
No
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: Laparoscopic tissue manipulation forceps/working-channel
Surgical Direct by Surgical Direct, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Laparoscopic tissue manipulation forceps/working-channel.
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- Ambler Surgical — Ambler Surgical, LLC · Class I
- Ambler Surgical — Ambler Surgical, LLC · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Surgical Direct, Inc.
Sources (1)
- FDA UDI 750653cb-10e2-4fef-834d-5a9b24c28ad5 35 fields · synced May 29, 2026