Flexible endoscopic biopsy forceps, single use - India CDSCO Medical Device Registration

Flexible endoscopic biopsy forceps, single use is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000059_1ce14c8dd696a524c29c7a918d13b035_8e7d0421ba2e1fcdf6748e8229e01575. This device is marketed under the brand name Interject Contrast Injection Therapy Needle Catheter. The license holder is Boston Scientific India Pvt. Ltd.,, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Flexible endoscopic biopsy forceps, single use

UID: IMP/MD/2018/000059_1ce14c8dd696a524c29c7a918d13b035_8e7d0421ba2e1fcdf6748e8229e01575

Brand Name

Interject Contrast Injection Therapy Needle Catheter

License Holder

Boston Scientific India Pvt. Ltd.,

Device Class

Class B

Approving Authority

CDSCO

Product Information

The SpyBite Max Single-Use Biopsy Forceps are designed to collect tissue samples endoscopically for histologic examination. These instruments should not be used for any purpose other than the intended function. The SpyBite Max Single-Use Biopsy Forceps are indicated for tissue acquisition in the pancreaticobiliary system