Medicon
- Primary DI
- 04046826063801
- Brand
- Medicon
- Company
- Medicon eG. Chirurgiemechaniker-Genossenschaft
- Model
- 52.01.04
- Catalog number
- 52.01.04
- Device description
- Cusco vag speculum 95x37mm
- Published
- 2020-09-24
- 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
Product Codes
| Code | Name |
|---|
| HDF | SPECULUM, VAGINAL, METAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| HDF | Speculum, Vaginal, Metal | Obstetrics/Gynecology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 04046826063801 | Primary | GS1 | 0 | |
Alternate GTIN/UPC/EAN values are derived from GS1 digit structure for lookup convenience. Do not treat derived UPC-A or EAN-13 values as separate FDA identifiers. GTIN-14 values with indicator digits 1-9 usually represent packaging levels, cases, pallets, or variable-measure items and are not converted to UPC-A/EAN-13 here.
Alternate GTIN / UPC / EAN Codes
| Source identifier | Source length | GTIN-14 normalized | Indicator | EAN-13 | Conversion note |
|---|
| 04046826063801 | 14 | 04046826063801 | 0 | 4046826063801 | Indicator 0 allows EAN-13 conversion; UPC-A requires prefix 00. |
GMDN Terms
| Term | Definition |
|---|
| Vaginal speculum, reusable | A hand-held manual instrument intended to dilate the vagina after insertion, typically for visual examination of the vaginal canal and cervix and/or to perform a gynaecological procedure. It consists of two long blades, joined at a handle at one end, that are inserted into the vagina in a horizontal position and then opened at an angle. It is typically made of stainless steel. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | Email |
|---|
| +490746220090 | sales@medicon.de |
Regulatory Flags
- DUNS number
- 315492330
- Device count
- 1
- DM exempt
- true
- 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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| 00198506087202 | ELMED INCORPORATED | ELMED INCORPORATED | HDF | 2025-12-18 |
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