Buying acetate frames in Bangladesh
Under EU guidance, a plastic spectacle frame has its rims, bridge, lugs and temples made only of synthetic or artificial materials, and cellulose acetate is one of the common ones. Brands and optical chains abroad buy acetate frames for colour and pattern; optical shops in Bangladesh sell them glazed with prescription lenses. An acetate frame manufacturer in Bangladesh has to hold colour, shape and size from sample to bulk.
Roptan takes one brief and sources from verified makers. We compare quotes on one material, hinge and test basis, keep your approved colours as the reference, check the lab reports and inspect the packed bulk.
How to specify an acetate frame
- Size
- Lens width, bridge and temple length in millimetres on the ISO 8624 boxing system, with tolerances, for each size you sell.
- Material part by part
- Name the material of the front, temples, core wires, hinges and screws. The answer decides whether the frame is plastic or combination, and which tests apply.
- Colours
- Give each colour a code and approve it on a physical sample. Keep a sealed approved sample per colour as the reference for the bulk.
- Hinges and temples
- Standard or spring hinge, and skull or library temples. Write the hinge type into the specification, since spring hinges have their own mechanical test.
- Heat
- Acetate is a thermoplastic, so ask for the dimensional stability test at elevated temperature, which matters for frames stored or shipped through hot months.
- Metal parts
- Ask for a nickel-release result on every metal part in skin contact, with its plating, even though the front is plastic.
Standards and rules for acetate frames
- ISO 12870:2024 (EN ISO 12870:2025)
- The current frame standard for unglazed frames for prescription lenses. The 2024 text also covers frames made by additive manufacturing and from natural organic materials.
- REACH nickel limit and EN 16128
- Metal parts in direct and prolonged skin contact may release at most 0.5 µg/cm² of nickel a week. EN 16128:2025 is the reference test for frames.
- EU medical device rules
- Spectacle frames are class I medical devices under Regulation (EU) 2017/745, normally self-declared, and the brand selling under its own name usually carries the manufacturer's duties.
- ISO 12312-1 for sun versions
- ISO 12870 does not cover plano sunglasses. An acetate frame sold with tinted plano lenses is tested as sunglasses instead.
Lead times and delivery
We give no figure here, because time depends on the order. It grows with a new shape, with many colours to approve, with spring hinges and metal parts to test, and with lab reports for each market. Roptan confirms the sample and bulk dates, and the minimum per model and colour, in the quote.
Inside Bangladesh we deliver to optical shops, chains, eye hospitals and distributors, sorted by model, size and colour code. Each delivery comes with the packing list, the frame and nickel reports and a VAT invoice (Mushak 6.3).
Buying acetate frames for export
For buyers abroad we ship by air from Hazrat Shahjalal International Airport, Dhaka, or FOB Chattogram for larger loads. Complete plastic frames usually go under HS 9003 11, parts and blanks under 9003 90. Papers include the certificate of origin, a REX statement for EU GSP or UK DCTS and the lab reports; the EU and UK want the importer's name and address on the product, its packaging or an accompanying document.
Questions buyers ask
Are acetate frames safe for people with a nickel allergy?
Do not assume so. The front may be plastic, but hinges, screws and core wires are usually metal and some touch the skin. For the EU those parts must meet the REACH nickel limit, so ask for a nickel report on each one.
Why test an acetate frame at raised temperature?
Cellulose acetate is a thermoplastic, which softens when heated. A frame that distorts in heat no longer sits straight or holds its lenses, so ISO 12870 includes a dimensional stability test at elevated temperature. Ask for it per model.
Can one acetate frame be sold as both optical and sun?
Yes, but the papers differ. Glazed with prescription lenses it is a frame under ISO 12870 and a class I medical device in the EU. With plano tinted lenses it is sunglasses under ISO 12312-1 and PPE. Plan both reports from the start.
Who is responsible for EU compliance under my brand?
Usually you. Under Article 16 of Regulation (EU) 2017/745, a company selling a device under its own name takes on the manufacturer's duties, unless an agreement names the maker on the label. From 1 November 2028 newly produced frames also need a Master UDI-DI.
How soon will I hear back about eyewear and optical?
Within 48 hours of a complete requirement, with a price and a delivery date. A requirement is complete when it has the quantity, where it is needed and by when.
Who do I deal with?
With Roptan, when Roptan manages the order: we buy from the verified seller and deliver to you. With the supplier directly, when you post on the requirement board and choose a quote yourself.