KES MED 808
KES MED 808 is a diode laser from Kes, identified by model/part reference KES MED 808. FDA/NLM AccessGUDID identifies KES MED-808, company Beijing KES Biology Technology Co., Ltd., with primary DI 06971513121046.
KES MED 808 product information
KES MED 808 is a diode laser from Kes, identified by model/part reference KES MED 808. FDA/NLM AccessGUDID identifies KES MED-808, company Beijing KES Biology Technology Co., Ltd., with primary DI 06971513121046.
For procurement, confirm the exact KES MED 808 label or serial identification, compatibility, included accessories and configuration against the written offer before installation or clinical/technical deployment.
Procurement focus
Match KES MED 808 model/part and serial or product-label details to the quotation.
Review host-system, accessory, software, power and facility requirements where relevant.
Confirm condition, included items, warranty, documentation and delivery terms before payment.
Important KES MED 808 details
These model-specific points help buyers evaluate identity, compatibility and purchasing requirements.
FDA/NLM AccessGUDID identifies KES MED-808, company Beijing KES Biology
FDA/NLM AccessGUDID identifies KES MED-808, company Beijing KES Biology Technology Co., Ltd., with primary DI 06971513121046.
The current KES manufacturer family page documents MED-808 hair-removal
The current KES manufacturer family page documents MED-808 hair-removal systems but newer configurations can use different wavelength/power options.
Use the exact physical model label and handpiece specification to distinguish
Use the exact physical model label and handpiece specification to distinguish the legacy MED-808 from later MED-808 MAX variants.
Where KES MED 808 can fit
Final suitability depends on the exact model configuration, compatible systems, professional use requirements and manufacturer instructions.
Professional laser workflow
Evaluate KES MED 808 for procedures specifically supported by the exact model, wavelength, handpiece and manufacturer documentation.
Clinic or surgical deployment
Confirm application-specific accessories, consumables, cooling, power and safety requirements before use.
System replacement or expansion
Useful where the exact laser platform and handpieces fit an established clinical or aesthetic workflow.
Safety and compliance
Laser classification, protective eyewear, plume control, training and local regulatory requirements should be reviewed before commissioning.
KES MED 808 specifications and identification
Use these details for product identification. Configuration-sensitive specifications should be checked against the exact supplied unit and manufacturer documentation.
- Product
- KES MED 808
- Manufacturer / brand
- Kes
- Equipment type
- Diode Laser
- Brand
- Kes
- Model / identifier
- MED 808
- Device
- MED 808
- Type
- Diode Laser
What to verify before ordering KES MED 808
Use this checklist to avoid configuration or compatibility mismatches.
- Exact model and wavelength/output label
- Software and operating-mode revision
- Handpieces/fibers/scanners/tips included
- Cooling and consumable requirements
- Output calibration and service history
- Destination-market labeling and intended-use requirements
KES MED 808 manufacturer and regulatory resources
Use authoritative documentation to confirm model identity, compatibility, operating requirements and configuration-sensitive details.
Regulatory document
Technical or regulatory resource relevant to KES MED 808 product evaluation.
Technical product resource
Technical or regulatory resource relevant to KES MED 808 product evaluation.
Frequently asked questions
Key questions for evaluating KES MED 808 before purchase.
What is KES MED 808?
KES MED 808 is a diode laser from Kes. FDA/NLM AccessGUDID identifies KES MED-808, company Beijing KES Biology Technology Co., Ltd., with primary DI 06971513121046.
What should be checked before ordering KES MED 808?
Exact model and wavelength/output label; Software and operating-mode revision; Handpieces/fibers/scanners/tips included.
Are all KES MED 808 configurations identical?
No. Hardware revision, software, accessories, probes, handpieces, modules or other options can vary. The written quotation and exact-unit identification should define the supplied configuration.
What is included with KES MED 808?
Only items explicitly listed in the quotation and packing scope should be treated as included. Reference photographs may show accessories or system components that are not part of the final offer.
Can KES MED 808 be shipped internationally?
International B2B delivery can be arranged for approved destinations subject to product-specific transport requirements, customs rules and the agreed Incoterms, freight and insurance conditions.
Kes documentation for KES MED 808
Manufacturer names and trademarks are used for product identification. Confirm model-specific instructions, compatibility and regional requirements before use.
Procurement support for KES MED 808
Model, label/serial information, condition and supplied configuration can be confirmed before dispatch.
Quotation, packing scope, warranty terms and delivery responsibilities are documented before order approval.
Export packing, freight, insurance and shipment documentation can be coordinated for approved destinations.
Support is available for configuration questions, installation planning and procurement documentation.
Request a KES MED 808 quote
Include delivery country, quantity, required configuration and target purchase date for a destination-specific offer.
