Gimmi
- Primary DI
- 04049047203155
- Brand
- Gimmi
- Company
- Gimmi GmbH
- Model
- E.8297.43 I
- Catalog number
- E.8297.43 I
- Device description
- CYSTOSCOPE/HYSTEROSCOPE 30° WORKING LENGTH 300 MM AUTOCLAVABLE, ALPHASCOPE II
- Published
- 2017-05-05
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| GCJ | Laparoscope, General & Plastic Surgery |
| HIH | HYSTEROSCOPE (AND ACCESSORIES) |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| GCJ | Laparoscope, General & Plastic Surgery | Gastroenterology, Urology | 2 |
| HIH | Hysteroscope (And Accessories) | Obstetrics/Gynecology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 04049047203155 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 04049047203155 | 04049047203155 | 4049047203155 |
GMDN Terms
| Term | Definition |
|---|
| Flexible fibreoptic cystoscope | An endoscope with a flexible inserted portion intended for the visual examination and treatment of the bladder and the urinary tract. It is inserted into the urethra (the tube that carries urine from the bladder to the outside of the body) through the natural urinary orifice during cystoscopy. Anatomical images are transmitted to the user by the device through a fibreoptic bundle. This device is commonly used to examine/diagnose incontinence, the inability to pass urine (retention), recurrent urinary tract infections, and to remove tissue samples/stones/small tumours from the bladder. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | Email |
|---|
| +497461965900 | contact@gimmi.de |
Regulatory Flags
- DUNS number
- 316152610
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- true
- 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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