Ultrapak E
- Primary DI
- 00883205003737
- Brand
- Ultrapak E
- Company
- ULTRADENT PRODUCTS, INC.
- Model
- 198
- Catalog number
- 198
- Device description
- Ultrapak E #0
- Published
- 2018-04-28
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MVL | CORD, RETRACTION |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MVL | Cord, Retraction | Unknown | U |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00883205003737 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00883205003737 | 00883205003737 | 883205003737 | 0883205003737 |
GMDN Terms#
| Term | Definition |
|---|---|
| Gingival retraction cord, non-medicated | A non-medicated, cotton string used to temporarily hold off the gingiva during abutment preparation. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(801)572-4200 | customerservice@ultradent.com |
Regulatory Flags#
- DUNS number
- 013369913
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- 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
- false
- Sterilization required before use
- false
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