Palium

Automatic Reusable GUN FOR Soft Tissues Biopsy, Palium Type

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (2), Zhejiang (1).

Chinese manufacturers registered for FDA product code FCG
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Promisemed Hangzhou Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 21
Suzhou Leapmed Healthcare Corporation Suzhou Jiangsu Contract manufacturer 3

Record

Regulatory record for Palium
Listed by M.D.L. S.R.L., Italy
FDA product code FCG
Device type Biopsy Needle
Device class Class 2
Regulation 21 CFR 876.1075
Establishment Contract manufacturer, Manufacturer
510(k) K160316
Record published 2021-05-17
Record revised 2025-03-06 (version 9)

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2021-05-14

Catalogue Numbers

Catalogue numbers for Palium
Catalogue number Size Status
PL In distribution
PL Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biopsybell Biopsybell SRL 227
Biopsybell SRL Biopsybell SRL 130
Medline Industries, Inc. Medline Industries, Inc. 98
Themy M.D.L. S.R.L. 61
SemiCut M.D.L. S.R.L. 46
Temno® Merit Medical Systems, Inc. 37
Temno Carefusion 2200, Inc. 36
CorVocet™ Merit Medical Systems, Inc. 34
Truguide Bard Peripheral Vascular, Inc. 31
Temno Evolution® Merit Medical Systems, Inc. 28
ClearTip Finemedix 25
Magnum Bard Peripheral Vascular, Inc. 22

Showing 12 of 115. All products under Biopsy Needle

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Palium
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
M.D.L. S.R.L. 510(k) number 2021-08-05 Class II Other Sterility assurance may be compromised. 20,129 units 2026-05-04

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