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ULTRATAPE Suture - Indonesia BPOM Medical Device Registration

ULTRATAPE Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324613. The device is manufactured by SMITH & NEPHEW, INC., ENDOSCOPY DIVISION (MANSFIELD) from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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BPOM Registered
Risk Class Kelas Resiko : C
ULTRATAPE Suture
Analysis ID: AKL 21603324613

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5

Registration Date

Sep 20, 2024

Expiry Date

Dec 31, 2027

Product Type

Surgical Equipment

Nonabsorbable poly(ethylene terephthalate) surgical suture.

Non Electromedic Non Sterile

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