Skip to content

Surshield MN*SVS23B18

by Terumo Medical Products (Hangzhou) Co., Ltd.

Surshield MN*SVS23B18 is a Class II device made by Terumo Medical Products (Hangzhou) Co., Ltd., listed in FDA GUDID since 12 Sep 2016 (UDI-DI 36927675503931), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number36927675503931 UDI-DI Date12 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Surshield
Generic name
Luer-ended blood collection tube spike
Model / Ref / Catalog
MN*SVS23B18
Primary DI / UDI-DI
36927675503931
FDA product code
FPA
GMDN term
Luer-ended blood collection tube spike
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 23 Gauge
Length — 0.75 Inch

Related devices

Category: Basic intravenous administration set, invasiveLuer-ended blood collection tube spike

Similar devices in this category

Other devices filed under Luer-ended blood collection tube spike.

Other devices from Terumo Medical Products (Hangzhou) Co., Ltd.

See all devices from Terumo Medical Products (Hangzhou) Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)