MINOP
- Primary DI
- 04046963888886
- Brand
- MINOP
- Company
- Aesculap AG
- Model
- FH637R
- Catalog number
- FH637R
- Device description
- MINOP inVent Micro Biopsy Forceps, working length: 10 1/2", (265 mm), diam. 2 mm, rotatable, with tubular shaft, ring handle, doubleaction, consisting of FF433R, FF437R, FH633R, detachable, reusable, to be used with: FH620R
- Published
- 2020-04-24
- 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
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| GZX | INSTRUMENT, MICROSURGICAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GZX | Instrument, Microsurgical | Neurology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046963888886 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046963888886 | 04046963888886 | 4046963888886 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical soft-tissue manipulation forceps, scissors-like, reusable | A hand-held, manual, open-surgery instrument designed to grasp, manipulate, dissect, and/or clamp soft-tissues (e.g., organs, blood vessels); it is not intended for grasping/clamping bone or teeth, nor is it dedicated to ophthalmic surgery and is not a dedicated biopsy device. It has a scissors-like hinged design with ring handles and blades (non-cutting) that may be available in a range of sizes or designs. It may be intended for use at a specific anatomy. This is a reusable device intended to be sterilized prior to use. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(800)282-9000 | GUDID.BBMUS_Service@bbraun.com |
Regulatory Flags
- DUNS number
- 315018218
- 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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