FRAENKEL LARYNGEAL FORCEPS
- Primary DI
- 00192896044166
- Brand
- FRAENKEL LARYNGEAL FORCEPS
- Company
- SONTEC INSTRUMENTS, INC.
- Model
- 502-277
- Catalog number
- 502-277
- Device description
- FRAENKEL LARYNGEAL FORCEPS FOREIGN BODY GRASPING DOUBLE ARTICULATING VERTICAL OPENING JAWS
- Published
- 2018-09-14
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| KAE | FORCEPS, ENT |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| KAE | Forceps, Ent | Ear, Nose, Throat | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00192896044166 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00192896044166 | 00192896044166 | 192896044166 | 0192896044166 |
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. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 9 | Inch |
Sterilization Methods
| Method |
|---|
| Dry Heat Sterilization;Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800) 821-7496 | info@sontecinstruments.com |
| +1(800)821-7496 | info@sontecinstruments.com |
Regulatory Flags
- DUNS number
- 040729840
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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