Identity
- Trade Name
- Ambler Surgical FDA UDI
- Generic Name
- Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
- Device Name
- Standard grasping forceps, 3-piece take apart, rotatable, double-action, 5.0mm diameter, 450.0mm working length, insulated shaft, straight tips, serrated jaws, carbon fiber ring handle with ratchet catch FDA UDI
- Model / Reference
- Standard grasping forceps FDA UDI
- Description
- Standard grasping forceps, 3-piece take apart, rotatable, double-action, 5.0mm diameter, 450.0mm working length, insulated shaft, straight tips, serrated jaws, carbon fiber ring handle with ratchet catch FDA UDI
Identifiers
- Catalog Number
- 97-007 FDA UDI
- Primary DI / UDI-DI
- 00190660205195 FDA UDI
- FDA Product Code
- GEN FDA UDI
- GMDN Term
- Rigid endoscopic tissue manipulation forceps, 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
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: Rigid endoscopic tissue manipulation forceps, reusable
Ambler Surgical by Ambler Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Ambler Surgical, LLC
Sources (1)
- FDA UDI 13fb5c8a-850f-4343-8c88-4858ac79bed4 35 fields · synced Jun 8, 2026