Aspen® Endoscopic Kittner, Single Tip
- Primary DI
- 10887761000008
- Brand
- Aspen® Endoscopic Kittner, Single Tip
- Company
- ASPEN SURGICAL PRODUCTS, INC.
- Model
- KT-9101
- Device description
- This product is single use and intended to be used for blunt dissection of tissue.
- Published
- 2016-09-17
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| GCJ | Laparoscope, general & plastic surgery |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | Gastroenterology, Urology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K913500 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10887761000008 | Package | GS1 | 20 | In Commercial Distribution |
| 00887761000001 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10887761000008 | 10887761000008 | ||
| 00887761000001 | 00887761000001 | 887761000001 | 0887761000001 |
GMDN Terms#
| Term | Definition |
|---|---|
| Dissection sponge | A sterile device intended to be used for blunt tissue dissection during a surgical procedure (e.g., from gross dissection to delicate neurological surgery). It typically consists of a small sponge made of hard but absorbent material (e.g., cotton twill, gauze, rayon) and frequently including an x-ray radiopaque element; some types include a hole in the centre to facilitate manipulation with forceps. It is available in a wide range of sizes and shapes (e.g., rosebud, peanut, cherry, round, Kittner). This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(616)698-7100 | customerservice@aspensurgical.com |
Regulatory Flags#
- DUNS number
- 027680821
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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