SWANN-MORTON - Skin Graft Blades - Indonesia BPOM Medical Device Registration
SWANN-MORTON - Skin Graft Blades is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603023560. The device is manufactured by SWANN-MORTON LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 1
Manufacturer
SWANN-MORTON LIMITEDCountry of Origin
United Kingdom
Authorized Representative
PT. LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
May 11, 2023
Expiry Date
Mar 01, 2026
Product Type
Surgical Equipment
Manual surgical instrument for general use.
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