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Byd Care DF1122

by BYD Precision Manufacture Co., Ltd.

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

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 Number00860003645154 UDI-DI Date6 Apr 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Byd Care
Generic Name
Surgical/examination garment kit
Model / Ref / Catalog
DF1122
Primary DI / UDI-DI
00860003645154
FDA Product Code
MSH
GMDN Term
Surgical/examination garment kit
Device Class
Class II
Regulation Number
878.4040
GUDID distribution status
In Commercial Distribution
Size
Circumference — 16.5 Inch

Related devices

Category: Surgical/examination garment kit

Other devices from BYD Precision Manufacture Co., Ltd.

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No