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AnchorFast Guard Select

FDA UDI

Class I (US FDA UDI)

by Hollister Incorporated

Identity

Trade Name
AnchorFast Guard Select FDA UDI
Generic Name
Endotracheal tube holder FDA UDI
Device Name
Oral Endotracheal Tube Fastener FDA UDI
Model / Reference
9700 FDA UDI
Description
Oral Endotracheal Tube Fastener FDA UDI

Identifiers

Catalog Number
9700 FDA UDI
Primary DI / UDI-DI
00610075095810 FDA UDI
FDA Product Code
CBH FDA UDI
GMDN Term
Endotracheal tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endotracheal tube holder

AnchorFast Guard Select by Hollister Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endotracheal tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c5518e5f-6e2e-4d74-8816-ebd097b7dbf1 35 fields · synced Jun 9, 2026