Medical Action Industries
- Primary DI
- 20809160169596
- Brand
- Medical Action Industries
- Company
- MEDICAL ACTION INDUSTRIES INC.
- Model
- 77636
- Published
- 2017-11-08
- Public version status
- Update
- Distribution status
- Not 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 |
|---|
| OGJ | Nerve block tray |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| OGJ | Nerve Block Tray | Anesthesiology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 20809160169596 | Package | GS1 | 20 | Not in Commercial Distribution |
| 10809160169599 | 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 | Conversion note |
|---|
| 20809160169596 | 14 | 20809160169596 | 2 | Indicator 2 usually represents packaging or variable measure; UPC/EAN conversion is not shown. |
| 10809160169599 | 14 | 10809160169599 | 1 | Indicator 1 usually represents packaging or variable measure; UPC/EAN conversion is not shown. |
GMDN Terms
| Term | Definition |
|---|
| Peripheral anaesthesia single-administration set, non-medicated | A collection of devices intended for the single-administration of an anaesthetic agent (not included) to function as a peripheral nerve-block; it is not dedicated to dental use. It includes an anaesthesia needle and a syringe often with additional devices utilized for the procedure (e.g., dressings); as a single-administration set it does not include a catheter. This is a single-use device. |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | |
| Special Storage Condition, Specify | 0 | 0 | STORE AT ROOM TEMPERATURE |
Regulatory Flags
- DUNS number
- 092364462
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- Combination product
- true
- 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
Other Devices From This Company
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|---|
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