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Nerbridge® RN02025E

by Toyobo Co., Ltd.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04965838907425 UDI-DI Date20 Apr 2018ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Nerbridge®
Generic Name
Nerve guide, animal-derived
Model / Ref / Catalog
RN02025E
Primary DI / UDI-DI
04965838907425
510(k) Number
FDA Product Code
JXI
GMDN Term
Nerve guide, animal-derived
Device Class
Class II
Regulation Number
882.5275
GUDID distribution status
Not in Commercial Distribution

Other devices from Toyobo Co., Ltd.

  • Nerbridge

    Class II

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No