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VersiTomic® ACL Flexible Reamer System Flexible Guide Pin

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name
VersiTomic® ACL Flexible Reamer System Flexible Guide Pin FDA UDI
Generic Name
Surgical drill guide, single-use FDA UDI
Model / Reference
234-108-200 FDA UDI

Identifiers

Catalog Number
tg108200st FDA UDI
Primary DI / UDI-DI
30810190018928 FDA UDI
FDA Product Code
GFG FDA UDI
GMDN Term
Surgical drill guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
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

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

Yes

FDA UDI

Category: Surgical drill guide, single-use

VersiTomic® ACL Flexible Reamer System Flexible Guide Pin by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA…

Similar devices

Also classified as Surgical drill guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24d03654-73c2-495b-93d1-e42dc4b1e1a2 33 fields · synced May 30, 2026