Reprocessed 2.7mm EndoScrub Sheath, 30 Deg

Catalogue number 19-12027, listed by Suretek Medical, United States, under Cannula, Sinus. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code KAM
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Record

Regulatory record for Reprocessed 2.7mm EndoScrub Sheath, 30 deg
Listed by Suretek Medical, United States
FDA product code KAM
Device type Cannula, Sinus
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Reprocessor
Premarket notification Exempt
Record published 2021-06-16
Record revised 2026-01-12 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Reprocessed 2.7mm EndoScrub Sheath, 30 deg
Catalogue number Size Status
19-12027 In distribution

Same Product Code

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Product Sold by Catalogue numbers
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Inka The Trustee for Kaiser Family Trust 4

Showing 12 of 59. All products under Cannula, Sinus

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer