ARROW
- Primary DI
- 30801902014635
- Brand
- ARROW
- Company
- TELEFLEX INCORPORATED
- Model
- IPN032963
- Catalog number
- CD-00001
- Device description
- Clear Fenestrated Drape with adhesive
- Published
- 2016-09-16
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| FYA | GOWN, SURGICAL |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FYA | Gown, Surgical | General, Plastic Surgery | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 30801902014635 | Package | GS1 | 200 | In Commercial Distribution |
| 00801902014634 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 30801902014635 | 30801902014635 | | |
| 00801902014634 | 00801902014634 | 801902014634 | 0801902014634 |
GMDN Terms
| Term | Definition |
|---|
| Patient surgical drape, single-use, sterile | A sterile, noninvasive flat sheet designed to cover a portion of a patient’s anatomy during a surgical procedure to isolate a specific anatomical site (e.g., site of surgical incision) from potential contamination (e.g., microbial, substance). The device may also be used to protect a patient from heat/flame during a surgical procedure, however it is not designed with specific heat-reflective or laser resistant materials. This is a single-use device. |
Regulatory Flags
- DUNS number
- 002348191
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- true
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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