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Grippies

FDA UDI

Class I (US FDA UDI)

by Salter Labs

Identity

Trade Name
Grippies FDA UDI
Generic Name
Universal patient tubing holder, non-sterile FDA UDI
Device Name
Grippies non-toxic hook and loop fastener strip (0.75" wide) FDA UDI
Model / Reference
GR102C-0-110 FDA UDI
Description
Grippies non-toxic hook and loop fastener strip (0.75" wide) FDA UDI

Identifiers

Catalog Number
GR102C-0-110 FDA UDI
Primary DI / UDI-DI
10607411007429 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Universal patient tubing holder, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 0.75 Inch FDA UDI

Category: Universal patient tubing holder, non-sterile

Grippies by Salter Labs — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal patient tubing holder, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Salter Labs

Sources (1)

  • FDA UDI bc03b4df-a590-4094-96a5-ca388d96bd55 36 fields · synced May 31, 2026