10 mL Cross-Linked Hyaluronic Acid Gel
A confirmed 10 mL hyaluronic acid gel presentation with a default cross-linked 20 mg/mL configuration in a large-volume prefilled syringe.
Public portfolio parameters
Current B2B portfolio baseline for initial format review.
- Net volume
- 10.0 mL per syringe
- Hyaluronic acid concentration
- 20 mg/mL
- Presentation
- Large-volume graduated prefilled syringe
- Cross-linking
- Monophasic (default); biphasic available for qualified B2B projects
- Storage
- Store at 2°C–25°C; protect from light; do not freeze.
- Shelf life
- 24 months
- Manufacturing entity
- GuangLong
Final release specifications, target-market documentation and any use claims remain subject to the qualified project review.
10 mL Cross-Linked Gel Configuration
The GuangLong 10 mL product is presented as a large-volume graduated prefilled syringe. The default project configuration is cross-linked hyaluronic acid gel, separating this format from smaller general presentation sizes and larger plastic-syringe options.
Confirmed Public Parameters
- Net volume: 10.0 mL per syringe
- Default configuration: Cross-linked hyaluronic acid gel at 20 mg/mL
- Primary presentation: Large-volume graduated prefilled syringe
- Manufacturing entity: GuangLong
- B2B coordination: Innovision Bio
Large-Volume Packaging Review
Qualified discussions address syringe material and connector, plunger travel, tray protection, pouch and carton construction, labeling language and destination-market requirements. The package visual is used to establish presentation scope before project-specific records are reviewed.
Information Confirmed Per Project
Final concentration, cross-linking specification, component references, sterilization records and applicable market documentation are confirmed against the buyer brief. No final IFU, registration or release specification is represented on this page.
Project review
Before requesting project-specific information
A concise brief helps us confirm the right commercial and documentation path for your discussion.
- Identify the target market, responsible entity, and intended professional channel.
- Describe the commercial scope, packaging concept, and indicative project timing.
- State the discussion stage and whether an NDA is already in place.
- Request only the information needed for the current qualified review stage.
Project-specific materials are considered only after qualification and do not represent product approval, registration, or a public technical specification.