FB3151-3 FLEXIBLE BIOPSY CUP FORCEP 1.6mm X 65CM
- Primary DI
- 00848657016384
- Brand
- FB3151-3 FLEXIBLE BIOPSY CUP FORCEP 1.6mm X 65CM
- Company
- NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
- Model
- FB3151-3
- Catalog number
- FB3151-3
- Device description
- A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastro-urological endoscopy, laparoscopy, bronchoscopy, laryngoscopy) for histopathological examination.
- Published
- 2023-04-24
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| GEN | Forceps, General & Plastic Surgery |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GEN | Forceps, General & Plastic Surgery | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00848657016384 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00848657016384 | 00848657016384 | 848657016384 | 0848657016384 |
GMDN Terms#
| Term | Definition |
|---|---|
| Flexible endoscopic biopsy forceps, reusable | A flexible, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., gastro-urological endoscopy, laparoscopy, bronchoscopy, laryngoscopy) for histopathological examination. It is typically a flexible metal coil with a pair of scissors-like cups with cutting edge rims, which are operated by a control handle at the proximal end of the instrument. It is introduced into the body through an artificial orifice of the body or the working channel of the endoscope. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +8182272720 | customerservice@aed.md |
Regulatory Flags#
- DUNS number
- 839138955
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
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