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CitreLock Inserter Large

FDA UDI

Class I (US FDA UDI)

by Acuitive Technologies

Identity

Trade Name
CitreLock Inserter Large FDA UDI
Generic Name
Surgical tamp, reusable FDA UDI
Model / Reference
40-102-0002 FDA UDI

Identifiers

Catalog Number
40-102-0002 FDA UDI
Primary DI / UDI-DI
00810027270139 FDA UDI
510(k) Number
K200725 FDA UDI
FDA Product Code
HXG FDA UDI
GMDN Term
Surgical tamp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical tamp, reusable

CitreLock Inserter Large by Acuitive Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical tamp, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d334c8df-0934-40c0-83eb-36c5950a02b6 35 fields · synced May 30, 2026