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Gryphon Brands

FDA UDI

Class I (US FDA UDI)

by Gryphon Brands Inc.

Identity

Trade Name
GRYPHON BRANDS FDA UDI
Generic Name
Surgical/examination garment kit FDA UDI
Model / Reference
VIN-4107-MD FDA UDI

Identifiers

Primary DI / UDI-DI
10810099841074 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Surgical/examination garment kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/examination garment kit

Gryphon Brands by Gryphon Brands Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/examination garment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gryphon Brands Inc.

Sources (1)

  • FDA UDI e092d5e4-32ed-4df4-80d3-bb009c9ae973 32 fields · synced May 30, 2026