Identity

Trade Name
HCS FDA UDI
Generic Name
Suture removal kit FDA UDI
Device Name
Staple Remover Kit FDA UDI
Model / Reference
HCS02STR-1 FDA UDI
Description
Staple Remover Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00849027003249 FDA UDI
GMDN Term
Suture removal kit FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture removal kit

Hcs by Dyad Medical Sourcing, Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture removal kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f1268f14-f199-4db7-8e0a-18ac56c5bea5 33 fields · synced May 30, 2026