# ReMedium 1 mL

> A hyaluronic-acid dermal filler (20 mg/mL, DVS cross-linked) with MDM Technology, a monophasic micro-bead gel. Fine, Mid and Sub-Q grades, with or without lidocaine.

- Page: https://allbeauty.app/product/remedium-1-ml
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- Brand: [ReMedium](https://allbeauty.app/brands/remedium.md)
- Manufacturer: Forever18 International Co., Ltd.
- Products: [Dermal Fillers](https://allbeauty.app/products/dermal-fillers.md)

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## Variants

| Variant | Longevity | Volume | Lidocaine |
| --- | --- | --- | --- |
| Fine | 12 months | 1 ml | Without lidocaine |
| Fine | 12 months | 1 ml | With lidocaine |
| Mid | 18 months | 1 ml | Without lidocaine |
| Mid | 18 months | 1 ml | With lidocaine |
| Sub-Q | 24 months | 1 ml | Without lidocaine |
| Sub-Q | 24 months | 1 ml | With lidocaine |

## Specifications

### Composition

- HA concentration: 20 mg/ml
- Cross-linking technology: Monophasic
- Contains lidocaine: Varies by Variant
- Cross-linking agent: DVS
- Lidocaine content: 0.3 %

### Treatment

- Injection depth: Intradermal, Subcutaneous
- Treatment areas: Nasolabial folds, Lips, Cheeks, Chin, Nose, Forehead, Neck, Hands, Scars
- Correction type: Fine lines, Volumizing, Contouring

### Regulatory

- Country of origin: South Korea
- Regulatory status: CE mark, KFDA (MFDS), GMP, ISO 13485

### Packaging

- Storage temperature: Room temperature (up to 25 °C)
- Pack size: 1 pcs
- Shelf life: 24 months

## ReMedium 1 mL: monophasic hyaluronic acid filler with MDM Technology

ReMedium is a hyaluronic acid (HA) dermal filler made in South Korea. It is supplied as one 1.0 mL syringe, with or without lidocaine, at an HA concentration of 20 mg/mL. The manufacturer describes it as combining viscoelasticity, long-lasting results and a high safety profile. It comes in three grades, Fine, Mid and Sub-Q. Each grade is available with lidocaine (3 mg/mL) and without lidocaine, so there are six variants.

## MDM Technology

The manufacturer states that ReMedium is based on its MDM technology, which has three parts:

- **MBMT (Micro Bead Monophasic Technology):** a monophasic gel made of aggregated micro-beads. The viscoelasticity can be adjusted to the purpose of use.
- **DMCT (Divinyl sulfone Multi Crosslink Technology):** the gel is cross-linked with divinyl sulfone (DVS) to raise viscoelastic efficiency. The manufacturer says DVS gives complete cross-linking and minimizes pendant cross-linker residue, compared with BDDE.
- **MDAP (Multiple Degree Amphiphilic Purification):** multi-stage purification that removes DVS residues. The manufacturer's test data show no detectable divinyl sulfone residue in the tested ReMedium Sub-Q Lidocaine samples.

## Specification

| Item | Value |
|---|---|
| HA concentration | 20 mg/mL |
| Lidocaine | 3 mg/mL (with or without) |
| Gel type | Monophasic |
| Cross-linking agent | DVS |
| Storage | 1-25 °C |
| Packaging | 1 syringe x 1.0 mL |
| Shelf life | 36 months |

## Grades

| | Fine | Mid | Sub-Q |
|---|---|---|---|
| Injection force | 20-25 N | 40-45 N | 50-55 N |
| Needle | 30G, 13 mm (ultra thin wall) | 27G, 13 mm (ultra thin wall) | 25G, 13 mm (ultra thin wall) |
| Injection depth | Dermis | Subcutaneous | Deep subcutaneous |
| Duration (manufacturer data) | 9-12 months | 12-18 months | 18-24 months |

The grades differ in cross-linking rate, viscoelasticity, moldability and cohesiveness. Fine has the lowest values on the manufacturer's scale and Sub-Q has the highest.

## Injection areas

The manufacturer's treatment map lists these areas by grade:

- **Fine:** glabella, crow's feet, perioral area, labial commissures, lips.
- **Mid:** temples, nose, cheeks, nasolabial folds, lips, marionette lines.
- **Sub-Q:** temples, nose, cheeks, nasolabial folds, jawline, chin, cheekbones, facial oval, marionette lines.

The manufacturer's before-and-after examples cover crow's feet, lip enlargement, jawline enlargement and nasolabial folds.

## Certification

The manufacturer lists these certificates and documents:

| Certificate | Scope |
|---|---|
| MDSAP | Quality management system certification for the US, Japan, Canada, Australia and Brazil |
| CE | European certification |
| EN ISO 13485 | Medical device quality management system certification (European) |
| GMP | Seongnam plant in Korea |
| DOC | Declaration of Conformity |

This product is for use by licensed practitioners only. Performance and duration figures are the manufacturer's statements.