ELEVATOR
- Primary DI
- 00888118059635
- Brand
- ELEVATOR
- Company
- KLS-Martin L.P.
- Model
- 37-568-21-07
- Published
- 2018-09-26
- Public version status
- Update
- 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 |
|---|---|
| KAD | ELEVATOR, ENT |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| KAD | Elevator, Ent | Ear, Nose, Throat | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118059635 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118059635 | 00888118059635 | 888118059635 | 0888118059635 |
GMDN Terms
| Term | Definition |
|---|---|
| ENT elevator | A hand-held, manually-operated, surgical instrument used to lift, position or pry anatomical structures or surgical material during ear/nose/throat (ENT) surgery. It may be a single or a double-ended device with a blunted blade or hook of various shapes with no cutting edges at the distal working end(s) and a handle positioned centrally or at the proximal end. Its shape and size depends upon the intended use, e.g., a blunt antrum, a rhinology or septum elevator, a strong nasal fracture elevator, or a specially designed ear elevator. It is usually made of high-grade stainless steel. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(904)641-7746 | KLS-UDI-Info@klsmartin.com |
Regulatory Flags
- DUNS number
- 826499238
- 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
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888118143266 | PURE PECTUS | 24-070-40-09 | 2026-03-23 | |
| 00888118143273 | PURE PECTUS | 24-070-42-09 | 2026-03-23 | |
| 00888118143280 | PURE PECTUS | 24-070-44-09 | 2026-03-23 | |
| 00888118143297 | PURE PECTUS | 24-070-46-09 | 2026-03-23 | |
| 00888118143303 | PURE PECTUS | 24-070-48-09 | 2026-03-23 | |
| 00888118143310 | PURE PECTUS | 24-070-50-09 | 2026-03-23 | |
| 00888118143327 | PURE PECTUS | 24-071-40-09 | 2026-03-23 | |
| 00888118143334 | PURE PECTUS | 24-071-42-09 | 2026-03-23 | |
| 00888118143341 | PURE PECTUS | 24-071-44-09 | 2026-03-23 | |
| 00888118143358 | PURE PECTUS | 24-071-46-09 | 2026-03-23 | |
| 00888118143365 | PURE PECTUS | 24-071-48-09 | 2026-03-23 | |
| 00888118143372 | PURE PECTUS | 24-071-50-09 | 2026-03-23 | |
| 00888118145321 | PURE PECTUS | 24-070-50-89 | 2026-03-23 | |
| 00888118145338 | PURE PECTUS | 24-071-50-89 | 2026-03-23 | |
| 00888118149671 | LEVEL ONE CMF, STERILE | 25-882-06-71 | 2026-03-23 | |
| 00888118149701 | LEVEL ONE CMF, STERILE | 25-883-17-71 | 2026-03-23 | |
| 00888118149718 | LEVEL ONE CMF, STERILE | 25-883-19-71 | 2026-03-23 | |
| 00888118149725 | LEVEL ONE CMF, STERILE | 25-887-17-71 | 2026-03-23 | |
| 00888118149732 | LEVEL ONE CMF, STERILE | 25-887-19-71 | 2026-03-23 | |
| 00888118149749 | LEVEL ONE CMF, STERILE | 25-889-09-71 | 2026-03-23 |
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